FDA 510(k)

CROSSFIRE SYSTEM 12 ACETABULAR INSERTS

K-Number: K993352 · 1999-11-19

Decision Date1999-11-19

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

CROSSFIRE SYSTEM 12 ACETABULAR INSERTS 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 1999-11-19 under 510(k) number K993352. 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 CROSSFIRE SYSTEM 12 ACETABULAR INSERTS?

CROSSFIRE SYSTEM 12 ACETABULAR INSERTS is a medical device that received FDA 510(k) clearance on 1999-11-19. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K993352.

When did CROSSFIRE SYSTEM 12 ACETABULAR INSERTS receive FDA 510(k) clearance?

CROSSFIRE SYSTEM 12 ACETABULAR INSERTS received FDA 510(k) clearance on 1999-11-19, under 510(k) number K993352.

Who is the listed applicant for CROSSFIRE SYSTEM 12 ACETABULAR INSERTS?

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 CROSSFIRE SYSTEM 12 ACETABULAR INSERTS?

The FDA product code for CROSSFIRE SYSTEM 12 ACETABULAR INSERTS is LPH.

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Related Devices (Code: 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.