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FDA 510(k)

Zimmer M/L Taper Hip Prosthesis

K-Number: K192660 · 2020-02-28

ApplicantZimmer, Inc.
Decision Date2020-02-28
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Zimmer M/L Taper Hip Prosthesis is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2020-02-28 under approval number K192660. 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 Zimmer M/L Taper Hip Prosthesis?

Zimmer M/L Taper Hip Prosthesis is a medical device that received FDA 510(k) clearance on 2020-02-28. It is manufactured by Zimmer, Inc.. The 510(k) number is K192660.

When was Zimmer M/L Taper Hip Prosthesis approved by the FDA?

Zimmer M/L Taper Hip Prosthesis received FDA 510(k) clearance on 2020-02-28, under approval number K192660.

What company makes Zimmer M/L Taper Hip Prosthesis?

Zimmer M/L Taper Hip Prosthesis is manufactured by Zimmer, Inc..

What is the FDA product code for Zimmer M/L Taper Hip Prosthesis?

The FDA product code for Zimmer M/L Taper Hip Prosthesis is LZO.

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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.