FDA 510(k)

TRIDENT ACETABULAR SYSTEM

K-Number: K033716 · 2005-02-10

Decision Date2005-02-10

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TRIDENT ACETABULAR SYSTEM 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 2005-02-10 under 510(k) number K033716. 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 ACETABULAR SYSTEM?

TRIDENT ACETABULAR SYSTEM is a medical device that received FDA 510(k) clearance on 2005-02-10. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K033716.

When did TRIDENT ACETABULAR SYSTEM receive FDA 510(k) clearance?

TRIDENT ACETABULAR SYSTEM received FDA 510(k) clearance on 2005-02-10, under 510(k) number K033716.

Who is the listed applicant for TRIDENT ACETABULAR SYSTEM?

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 ACETABULAR SYSTEM?

The FDA product code for TRIDENT ACETABULAR SYSTEM 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.