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FDA 510(k)

Arthrex Virtual Implant Positioning (VIP) System

K-Number: K230904 · 2023-06-22

ApplicantArthrex, Inc.
Decision Date2023-06-22
Product CodeQHE
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Arthrex Virtual Implant Positioning (VIP) System is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2023-06-22 under 510(k) number K230904. The device is classified under product code QHE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arthrex Virtual Implant Positioning (VIP) System?

Arthrex Virtual Implant Positioning (VIP) System is a medical device that received FDA 510(k) clearance on 2023-06-22. The listed applicant is Arthrex, Inc.. The 510(k) number is K230904.

When did Arthrex Virtual Implant Positioning (VIP) System receive FDA 510(k) clearance?

Arthrex Virtual Implant Positioning (VIP) System received FDA 510(k) clearance on 2023-06-22, under 510(k) number K230904.

Who is the listed applicant for Arthrex Virtual Implant Positioning (VIP) System?

The FDA 510(k) record lists Arthrex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Arthrex Virtual Implant Positioning (VIP) System?

The FDA product code for Arthrex Virtual Implant Positioning (VIP) System is QHE.

Other records listing Arthrex, Inc. as applicant

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Related Devices (Code: QHE)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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