FDA 510(k)

ZIMMER M/L TAPER HIP PROSTHESIS, 7711 SERIES

K-Number: K032726 · 2003-10-22

Decision Date2003-10-22

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ZIMMER M/L TAPER HIP PROSTHESIS, 7711 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2003-10-22 under 510(k) number K032726. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIMMER M/L TAPER HIP PROSTHESIS, 7711 SERIES?

ZIMMER M/L TAPER HIP PROSTHESIS, 7711 SERIES is a medical device that received FDA 510(k) clearance on 2003-10-22. The listed applicant is Zimmer, Inc.. The 510(k) number is K032726.

When did ZIMMER M/L TAPER HIP PROSTHESIS, 7711 SERIES receive FDA 510(k) clearance?

ZIMMER M/L TAPER HIP PROSTHESIS, 7711 SERIES received FDA 510(k) clearance on 2003-10-22, under 510(k) number K032726.

Who is the listed applicant for ZIMMER M/L TAPER HIP PROSTHESIS, 7711 SERIES?

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

What is the FDA product code for ZIMMER M/L TAPER HIP PROSTHESIS, 7711 SERIES?

The FDA product code for ZIMMER M/L TAPER HIP PROSTHESIS, 7711 SERIES is LPH.

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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.