ArthrexVIP
Medical
Free
iPad
The VIP™ preoperative planning system is a medical device designed to facilitate the transfer of information between surgeons and Arthrex technicians. With purposeful functionality, the application allow surgeons to make adjustments to protocol-based plans created by Arthrex technicians. Once the initial plan is created, a surgeon can adjust an implant’s position and orientation on the isolated scapula in both 2D and 3D within the ArthrexVIP application. The application also serves as a communication channel between surgeons and technicians through the approval process. Once a plan is approved in the application, further changes are prohibited.
Key Features:
View bones and implants in 3D as well as orthographic 2D cross sections
Display/adjust plans created by Arthrex technicians
Comments function that allows surgeons and technicians to communicate
Perform angle and length measurements in 2D views
Surgeons can approve preoperative plans by typing their password into the application
Snap the view of the 3D model to anatomic reference planes (anterior, posterior, inferior, superior)
Adjust the type and size of the implant that was chosen by the Arthrex technician
Show/hide 3D model components (guide pin, implant, bone)
Show the original CT slices in the 2D and 3D views
Adjust the transparency of the bone and implant in the 3D view from 0% to 100% visibility
View articulating surfaces for both anatomic and reverse total shoulder replacements
View and select locking and non-locking screw trajectories for baseplates with screw options
View backside seating coverage of the implant with the patient anatomy
View maximum gap and maximum depth of the implant into the patient anatomy
View planned postoperative deviation from the native center of rotation
View preoperative native volumetric humeral head subluxation
About Arthrex
Arthrex is a global medical device company and leader in new product development and medical education in orthopedics. With a corporate mission of Helping Surgeons Treat Their Patients Better™, Arthrex has pioneered the field of arthroscopy and develops more than 1,000 innovative products and procedures each year.
Arthrex continues to experience unprecedented growth and demand for our products throughout the world; however, we remain a privately held company with a family business culture committed to delivering uncompromising quality to the health care professionals who use our products, and ultimately, the millions of patients whose lives we impact.
We invite you to learn more about Arthrex and the positive contributions we are making to medicine and the communities we serve. Please visit us at www.arthrex.com.
Ratings & Reviews
Version 9.2.1. Hotfix release for bug fixes for the plan viewer not loading for cases in the EEA database, an incorrect metal cases approval message, an incorrect case deletion badge, an upgrade of the OrthoVis dicom library, and cybersecurity fixes.
The developer, Arthrex, Inc., indicated that the app’s privacy practices may include handling of data as described below. For more information, see the developer’s privacy policy .
Data Linked to You
The following data may be collected and linked to your identity:
- Identifiers
Data Not Linked to You
The following data may be collected but it is not linked to your identity:
- Usage Data
- Diagnostics
Accessibility
The developer has not yet indicated which accessibility features this app supports. Learn More
Information
- Seller
- ARTHREX CALIFORNIA TECHNOLOGY INC.
- Size
- 285.9 MB
- Category
- Medical
- Compatibility
Requires iPadOS 15.0 or later and a device with the A12 Bionic chip or later.
- iPad
Requires iPadOS 15.0 or later and a device with the A12 Bionic chip or later.
• iPad Pro (11‑inch)
• iPad Pro (11‑inch) Wi‑Fi + Cellular
• iPad Pro (12.9‑inch) (3rd generation)
• iPad Pro (12.9‑inch) (3rd generation) Wi‑Fi + Cellular
• iPad mini (5th generation)
• iPad mini (5th generation) Wi‑Fi + Cellular
• iPad Air (3rd generation)
• iPad Air (3rd generation) Wi‑Fi + Cellular
• iPad Pro (11‑inch) (2nd generation)
• iPad Pro (11‑inch) (2nd generation) Wi‑Fi + Cellular
• iPad Pro (12.9‑inch) (4th generation)
• iPad Pro (12.9‑inch) (4th generation) Wi‑Fi + Cellular
• iPad Air (4th generation)
• iPad Air (4th generation) Wi‑Fi + Cellular
• iPad (8th generation)
• iPad (8th generation) Wi‑Fi + Cellular
• iPad Pro (11-inch) (3rd generation)
• iPad Pro (11-inch) (3rd generation) Wi‑Fi + Cellular
• iPad Pro (12.9-inch) (5th generation)
• iPad Pro (12.9-inch) (5th generation) Wi-Fi + Cellular
• iPad mini (6th generation)
• iPad mini (6th generation) Wi-Fi + Cellular
• iPad (9th generation)
• iPad (9th generation) Wi-Fi + Cellular
• iPad Air (5th generation)
• iPad Air (5th generation) Wi‑Fi + Cellular
• iPad (10th generation)
• iPad (10th generation) Wi‑Fi + Cellular
• iPad Pro (11‑inch) (4th generation)
• iPad Pro (11‑inch) (4th generation) Wi‑Fi + Cellular
• iPad Pro (12.9‑inch) (6th generation)
• iPad Pro (12.9‑inch) (6th generation) Wi‑Fi + Cellular
• iPad Air 11-inch (M2)
• iPad Air 11-inch (M2) Wi-Fi + Cellular
• iPad Air 13-inch (M2)
• iPad Air 13-inch (M2) Wi-Fi + Cellular
• iPad Pro 11-inch (M4)
• iPad Pro 11-inch (M4) Wi-Fi + Cellular
• iPad Pro 13-inch (M4)
• iPad Pro 13-inch (M4) Wi-Fi + Cellular
• iPad mini (A17 Pro)
• iPad mini (A17 Pro) Wi-Fi + Cellular
• iPad (A16)
• iPad (A16) Wi-Fi + Cellular
• iPad Air 11-inch (M3)
• iPad Air 11-inch (M3) Wi-Fi + Cellular
• iPad Air 13-inch (M3)
• iPad Air 13-inch (M3) Wi-Fi + Cellular
• iPad Pro 11-inch (M5)
• iPad Pro 11-inch (M5) Wi-Fi + Cellular
• iPad Pro 13-inch (M5)
• iPad Pro 13-inch (M5) Wi-Fi + Cellular
• iPad Air 11-inch (M4)
• iPad Air 11-inch (M4) Wi-Fi + Cellular
• iPad Air 13-inch (M4)
• iPad Air 13-inch (M4) Wi-Fi + Cellular
- iPad
- Languages
- English
- Age Rating
16+
- 16+
- Frequent
Medical Treatment information
- Medical Device
Yes
- Arthrex, Inc. indicated this app is a regulated medical device and complies with United States law.
- The information below has not been verified by Apple.
- FDA Owner/Operator Number
- 1220287
- Address
- 460 Ward Dr
Santa Barbara California 93111
United States - Phone Number
- +1 720-938-1383
- gregory.st.clair@arthrex.com
- Use Statement
- VIP Web Portal:
The VIP Web Portal is intended for use as a software interface and for the transfer of imaging information from a medical scanner such as a CT scanner. It is also intended as software for displaying/editing implant placement and surgical treatment options that were generated in the OrthoVis desktop software by trained Arthrex technicians.
The VIP Web Portal is intended for use with the VIP glenoid instrumentation and with the OrthoVis preoperative plan. It is indicated for use with the following implant lines: Univers II and Univers Apex total shoulder systems, keeled or pegged glenoid components, the Univers VaultLock glenoid component, as well as the Univers Revers baseplate component (Universal Glenoid), Univers Revers modular glenoid system (MGS) baseplates, and Arthrex humeral implants compatible with these implant lines.
OrthoVis Preoperative Plan:
The OrthoVis Preoperative Plan is a preoperative plan created via the OrthoVis software that facilitates accurate preoperative planning of glenoid and humeral components in total shoulder replacement, and intraoperative placement of the glenoid component in total shoulder replacement.
- Safety Information
- CONTRAINDICATIONS
1. The Arthrex VIP instrumentation and OrthoVis preoperative plan are not to be used with any shoulder replacement system or component other than the total shoulder systems and components identified in the Indications for Use of the VIP system.
2. The contraindications for the total shoulder systems with which the Arthrex VIP instrumentation and OrthoVis preoperative plan are indicated for use remain the same as those described in each implant system’s labeling.
3. The glenoid targeter should not be used if the legs of the instrument are not stable or move when locking nut is tightened and used for guide pin placement, and the failure should be reported to Arthrex.
4. If the seating of the glenoid targeter instrument on the patient cannot be exactly matched with the seating of the instrument on the glenoid 3D model, the surgeon must choose to either address the issue so that the glenoid targeter instrument seating is matched between the patient and the glenoid 3D model or alternatively, refrain from using the glenoid targeter.
5. The glenoid targeter is not indicated for use in hemi-shoulder arthroplasty.
Contraindications for Glenoid Targeter with Glenoid 3D Model
1. The glenoid targeter should not be used with the glenoid 3D model if the patient’s glenoid does not appear to the surgeon to be accurately represented in shape and size of the glenoid 3D model and the surgeon cannot or does not elect to make changes to the patient’s anatomy to accurately correspond to the glenoid 3D model.
2. If the location or trajectory of the guide pin in the glenoid 3D model does not match the intended/planned location or trajectory of the guide pin, do not use the Arthrex glenoid targeter.
WARNINGS
1. Caution: Federal law restricts this device to sale by or on the order of a physician.
2. This device is intended to be used by a trained medical professional.
3. Biohazard waste, such as explanted devices, needles, and contaminated surgical equipment, should be safely disposed of in accordance with the institution’s policy.
4. Serious incidents should be reported to Arthrex Inc., or an in-country representative, and to the health authority where the incident occurred.
- Instructions for Use
- Visit the developer site
- Copyright
- © 2025 Arthrex
