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FDA 510(k)

Zimmer Segmental System Proximal Femoral Component

K-Number: K183136 · 2019-01-30

ApplicantZimmer, Inc.
Decision Date2019-01-30
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Zimmer Segmental System Proximal Femoral Component is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2019-01-30 under approval number K183136. 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 Segmental System Proximal Femoral Component?

Zimmer Segmental System Proximal Femoral Component is a medical device that received FDA 510(k) clearance on 2019-01-30. It is manufactured by Zimmer, Inc.. The 510(k) number is K183136.

When was Zimmer Segmental System Proximal Femoral Component approved by the FDA?

Zimmer Segmental System Proximal Femoral Component received FDA 510(k) clearance on 2019-01-30, under approval number K183136.

What company makes Zimmer Segmental System Proximal Femoral Component?

Zimmer Segmental System Proximal Femoral Component is manufactured by Zimmer, Inc..

What is the FDA product code for Zimmer Segmental System Proximal Femoral Component?

The FDA product code for Zimmer Segmental System Proximal Femoral Component 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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