FDA 510(k)

TRIDENT ELEVATED RIM LINER

K-Number: K020497 · 2002-03-04

Decision Date2002-03-04

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TRIDENT ELEVATED RIM LINER is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 2002-03-04 under 510(k) number K020497. 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 TRIDENT ELEVATED RIM LINER?

TRIDENT ELEVATED RIM LINER is a medical device that received FDA 510(k) clearance on 2002-03-04. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K020497.

When did TRIDENT ELEVATED RIM LINER receive FDA 510(k) clearance?

TRIDENT ELEVATED RIM LINER received FDA 510(k) clearance on 2002-03-04, under 510(k) number K020497.

Who is the listed applicant for TRIDENT ELEVATED RIM LINER?

The FDA 510(k) record lists Howmedica Osteonics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRIDENT ELEVATED RIM LINER?

The FDA product code for TRIDENT ELEVATED RIM LINER 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.