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FDA 510(k)

REPICCI LOCKED KEEL TIBIAL BEARING

K-Number: K030446 · 2003-03-06

ApplicantBiomet, Inc.
Decision Date2003-03-06
Product CodeHRY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

REPICCI LOCKED KEEL TIBIAL BEARING is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2003-03-06 under 510(k) number K030446. The device is classified under product code HRY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPICCI LOCKED KEEL TIBIAL BEARING?

REPICCI LOCKED KEEL TIBIAL BEARING is a medical device that received FDA 510(k) clearance on 2003-03-06. The listed applicant is Biomet, Inc.. The 510(k) number is K030446.

When did REPICCI LOCKED KEEL TIBIAL BEARING receive FDA 510(k) clearance?

REPICCI LOCKED KEEL TIBIAL BEARING received FDA 510(k) clearance on 2003-03-06, under 510(k) number K030446.

Who is the listed applicant for REPICCI LOCKED KEEL TIBIAL BEARING?

The FDA 510(k) record lists Biomet, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPICCI LOCKED KEEL TIBIAL BEARING?

The FDA product code for REPICCI LOCKED KEEL TIBIAL BEARING is HRY.

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Related Devices (Code: HRY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K193549SIGMA High Performance (HP) Partial Knee SystemDepuy Ireland UCK190633NanoOrtho NanoKnee® SystemNanoortho, LLCK152631MPO Total Knee Systems MR LabelingMicroport Orthopedics, Inc.K131167UNIVATIONAesculap Implant Systems, LLCK122277OXFORD FIXED LATERAL BEARING PARTIAL KNEE REPLACEMENT (OXFORD TIBIAL TRAYS A-F) IXFORD PARTIAL KNEE REPLACEMENT SYSTEMBiomet Manufacturing CorpK110415SIGNATURE PLANNER / SIGNATURE GUIDESMaterialise NV

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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