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FDA 510(k)

Exactech® Vantage® Total Ankle System

K-Number: K230717 · 2023-10-12

Decision Date2023-10-12
Product CodeHSN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Exactech® Vantage® Total Ankle System is the device name listed in this FDA 510(k) record. The listed applicant is Exactech, Inc.. It received FDA 510(k) clearance on 2023-10-12 under 510(k) number K230717. The device is classified under product code HSN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Exactech® Vantage® Total Ankle System?

Exactech® Vantage® Total Ankle System is a medical device that received FDA 510(k) clearance on 2023-10-12. The listed applicant is Exactech, Inc.. The 510(k) number is K230717.

When did Exactech® Vantage® Total Ankle System receive FDA 510(k) clearance?

Exactech® Vantage® Total Ankle System received FDA 510(k) clearance on 2023-10-12, under 510(k) number K230717.

Who is the listed applicant for Exactech® Vantage® Total Ankle System?

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

What is the FDA product code for Exactech® Vantage® Total Ankle System?

The FDA product code for Exactech® Vantage® Total Ankle System is HSN.

Other records listing Exactech, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 41 devices →

Related Devices (Code: HSN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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