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FDA 510(k)

VALOR ANKLE FUSION NAIL SYSTEM

K-Number: K090857 · 2009-07-14

ApplicantWrightmedicaltechnologyinc
Decision Date2009-07-14
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VALOR ANKLE FUSION NAIL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2009-07-14 under 510(k) number K090857. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALOR ANKLE FUSION NAIL SYSTEM?

VALOR ANKLE FUSION NAIL SYSTEM is a medical device that received FDA 510(k) clearance on 2009-07-14. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K090857.

When did VALOR ANKLE FUSION NAIL SYSTEM receive FDA 510(k) clearance?

VALOR ANKLE FUSION NAIL SYSTEM received FDA 510(k) clearance on 2009-07-14, under 510(k) number K090857.

Who is the listed applicant for VALOR ANKLE FUSION NAIL SYSTEM?

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

What is the FDA product code for VALOR ANKLE FUSION NAIL SYSTEM?

The FDA product code for VALOR ANKLE FUSION NAIL SYSTEM is HSB.

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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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