FDA 510(k)

Physica LMC Knee System

K-Number: K211938 · 2021-07-13

Decision Date2021-07-13

Product CodeJWH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Physica LMC Knee System is a medical device manufactured by Limacorporate. It received FDA 510(k) clearance on 2021-07-13 under approval number K211938. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Physica LMC Knee System?

Physica LMC Knee System is a medical device that received FDA 510(k) clearance on 2021-07-13. It is manufactured by Limacorporate. The 510(k) number is K211938.

When was Physica LMC Knee System approved by the FDA?

Physica LMC Knee System received FDA 510(k) clearance on 2021-07-13, under approval number K211938.

What company makes Physica LMC Knee System?

Physica LMC Knee System is manufactured by Limacorporate.

What is the FDA product code for Physica LMC Knee System?

The FDA product code for Physica LMC Knee System is JWH.

Other Devices by Limacorporate

K190911Physica KR Liner and SMR Reverse Humeral Liner K213785SMR TT Hybrid Glenoid, SMR 3-Pegs Cemented Glenoid K243809Biolox® Delta Revision heads

Related Devices (Code: JWH)

K160515PS2 Knee SystemConsensus Orthopedics, Inc. K160771Destiknee Total Knee SystemMeril Healthcare Private Limited K160157LOSPA Modular Knee SystemCorentec Co., Ltd. K162273Materialise TKA Guide SystemMaterialise NV K162422Klassic Knee SystemTotal Joint Orthopedics, Inc. K161945EXPRT Revision Knee Femoral Augment(5mm), EXPRT Revision Knee Stem Extension (40mm)Encore Medical L.P.

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.