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FDA 510(k)

TRIDENT ACETABULAR SHELLS: PS

K-Number: K001449 · 2000-08-04

ApplicantHowmedica Osteonics Corp.
Decision Date2000-08-04
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRIDENT ACETABULAR SHELLS: PS 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 2000-08-04 under 510(k) number K001449. 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 TRIDENT ACETABULAR SHELLS: PS?

TRIDENT ACETABULAR SHELLS: PS is a medical device that received FDA 510(k) clearance on 2000-08-04. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K001449.

When did TRIDENT ACETABULAR SHELLS: PS receive FDA 510(k) clearance?

TRIDENT ACETABULAR SHELLS: PS received FDA 510(k) clearance on 2000-08-04, under 510(k) number K001449.

Who is the listed applicant for TRIDENT ACETABULAR SHELLS: PS?

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 SHELLS: PS?

The FDA product code for TRIDENT ACETABULAR SHELLS: PS is LZO.

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Related Devices (Code: 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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