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FDA 510(k)

DYNASTY CERAMIC FEMORAL HEAD

K-Number: K072656 · 2008-02-06

ApplicantWrightmedicaltechnologyinc
Decision Date2008-02-06
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DYNASTY CERAMIC FEMORAL HEAD is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2008-02-06 under 510(k) number K072656. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNASTY CERAMIC FEMORAL HEAD?

DYNASTY CERAMIC FEMORAL HEAD is a medical device that received FDA 510(k) clearance on 2008-02-06. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K072656.

When did DYNASTY CERAMIC FEMORAL HEAD receive FDA 510(k) clearance?

DYNASTY CERAMIC FEMORAL HEAD received FDA 510(k) clearance on 2008-02-06, under 510(k) number K072656.

Who is the listed applicant for DYNASTY CERAMIC FEMORAL HEAD?

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 DYNASTY CERAMIC FEMORAL HEAD?

The FDA product code for DYNASTY CERAMIC FEMORAL HEAD is LZO.

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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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