Class Class II

Arthrex Virtual Implant Positioning (VIP) System Software (K241097)

K241097 2024-10-02 Traditional
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Description

Arthrex Virtual Implant Positioning (VIP) System Software by Arthrex, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241097
Clearance Date2024-10-02
Clearance TypeTraditional
Product CodeQHE
Regulation Number888.3660

Categories

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Predicate lineage for K241097

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 Software (K241097) cites 2 predicate devices and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K232265BLUEPRINT™ Patient Specific InstrumentationTornier S.A.S.2024
K230904Arthrex Virtual Implant Positioning (VIP) SystemArthrex, Inc.2023

Trace the full predicate network for K241097

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.

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