FDA 510(k)

TRILOGY ACETABULAR SHELL & LINERS 36MM

K-Number: K953490 · 1995-10-20

Decision Date1995-10-20

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TRILOGY ACETABULAR SHELL & LINERS 36MM is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1995-10-20 under 510(k) number K953490. 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 TRILOGY ACETABULAR SHELL & LINERS 36MM?

TRILOGY ACETABULAR SHELL & LINERS 36MM is a medical device that received FDA 510(k) clearance on 1995-10-20. The listed applicant is Zimmer, Inc.. The 510(k) number is K953490.

When did TRILOGY ACETABULAR SHELL & LINERS 36MM receive FDA 510(k) clearance?

TRILOGY ACETABULAR SHELL & LINERS 36MM received FDA 510(k) clearance on 1995-10-20, under 510(k) number K953490.

Who is the listed applicant for TRILOGY ACETABULAR SHELL & LINERS 36MM?

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 TRILOGY ACETABULAR SHELL & LINERS 36MM?

The FDA product code for TRILOGY ACETABULAR SHELL & LINERS 36MM is LPH.

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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.