Class Class II
Arthrex Virtual Implant Positioning (VIP) System (K222007)
Description
Arthrex Virtual Implant Positioning (VIP) System by Arthrex, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK222007
Clearance Date2023-03-08
Clearance TypeTraditional
Product CodeQHE
Regulation Number888.3660
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K222007
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Arthrex Virtual Implant Positioning (VIP) System (K222007) cites 3 predicate devices and is itself cited by 2 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K212560 | Signature ONE System | Orthosoft Inc (D/B/A Zimmer Cas) | 2021 |
| K193523 | ArthrexVIP Web Portal | Arthrex, Inc. | 2020 |
| K162697 | Arthrex Glenoid Intelligent Reusable Instrument System, Art... | Custom Orthopaedic Solutions, Inc. | 2017 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K241470 | CORE Shoulder System | LinkBio Corp. | 2025 |
| K230904 | Arthrex Virtual Implant Positioning (VIP) System | Arthrex, Inc. | 2023 |
Trace the full predicate network for K222007
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.