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FDA 510(k)

UNI KNEE

K-Number: K022437 · 2002-08-23

ApplicantEncore Medical L.P.
Decision Date2002-08-23
Product CodeHRY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

UNI KNEE is the device name listed in this FDA 510(k) record. The listed applicant is Encore Medical L.P.. It received FDA 510(k) clearance on 2002-08-23 under 510(k) number K022437. 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 UNI KNEE?

UNI KNEE is a medical device that received FDA 510(k) clearance on 2002-08-23. The listed applicant is Encore Medical L.P.. The 510(k) number is K022437.

When did UNI KNEE receive FDA 510(k) clearance?

UNI KNEE received FDA 510(k) clearance on 2002-08-23, under 510(k) number K022437.

Who is the listed applicant for UNI KNEE?

The FDA 510(k) record lists Encore Medical L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNI KNEE?

The FDA product code for UNI KNEE is HRY.

Other records listing Encore Medical L.P. as applicant

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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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