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FDA 510(k)

TRIDENT ALL POLY CUP

K-Number: K001956 · 2000-12-11

ApplicantHowmedica Osteonics Corp.
Decision Date2000-12-11
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRIDENT ALL POLY CUP 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 2000-12-11 under 510(k) number K001956. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIDENT ALL POLY CUP?

TRIDENT ALL POLY CUP is a medical device that received FDA 510(k) clearance on 2000-12-11. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K001956.

When did TRIDENT ALL POLY CUP receive FDA 510(k) clearance?

TRIDENT ALL POLY CUP received FDA 510(k) clearance on 2000-12-11, under 510(k) number K001956.

Who is the listed applicant for TRIDENT ALL POLY CUP?

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 ALL POLY CUP?

The FDA product code for TRIDENT ALL POLY CUP is JDI.

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Related Devices (Code: JDI)

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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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