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FDA 510(k)

VANGUARD M SERIES UNICONDYLAR TIBIAL BEARINGS

K-Number: K042093 · 2004-11-01

ApplicantBiomet, Inc.
Decision Date2004-11-01
Product CodeHRY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VANGUARD M SERIES UNICONDYLAR TIBIAL BEARINGS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2004-11-01 under 510(k) number K042093. 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 VANGUARD M SERIES UNICONDYLAR TIBIAL BEARINGS?

VANGUARD M SERIES UNICONDYLAR TIBIAL BEARINGS is a medical device that received FDA 510(k) clearance on 2004-11-01. The listed applicant is Biomet, Inc.. The 510(k) number is K042093.

When did VANGUARD M SERIES UNICONDYLAR TIBIAL BEARINGS receive FDA 510(k) clearance?

VANGUARD M SERIES UNICONDYLAR TIBIAL BEARINGS received FDA 510(k) clearance on 2004-11-01, under 510(k) number K042093.

Who is the listed applicant for VANGUARD M SERIES UNICONDYLAR TIBIAL BEARINGS?

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 VANGUARD M SERIES UNICONDYLAR TIBIAL BEARINGS?

The FDA product code for VANGUARD M SERIES UNICONDYLAR TIBIAL BEARINGS 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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