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FDA 510(k)

Physica System (Physica CR Porous Femoral components)

K-Number: K250980 · 2025-05-22

ApplicantLima Corporate S.P.A.
Decision Date2025-05-22
Product CodeMBH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Physica System (Physica CR Porous Femoral components) is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2025-05-22 under approval number K250980. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Physica System (Physica CR Porous Femoral components)?

Physica System (Physica CR Porous Femoral components) is a medical device that received FDA 510(k) clearance on 2025-05-22. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K250980.

When was Physica System (Physica CR Porous Femoral components) approved by the FDA?

Physica System (Physica CR Porous Femoral components) received FDA 510(k) clearance on 2025-05-22, under approval number K250980.

What company makes Physica System (Physica CR Porous Femoral components)?

Physica System (Physica CR Porous Femoral components) is manufactured by Lima Corporate S.P.A..

What is the FDA product code for Physica System (Physica CR Porous Femoral components)?

The FDA product code for Physica System (Physica CR Porous Femoral components) is MBH.

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Related Devices (Code: MBH)

K162256Klassic Femur, Porous, Klassic Tibial Baseplate, PorousTotal Joint Orthopedics, Inc. K153657Vanguard XP Knee SystemBiomet, Inc. K153776Optetrak One Logic Femoral ComponentsExactech, Inc. K153586Arthrex iBalance TKA SystemArthrex, Inc. K172634Triathlon® X3® UHMWPE Tibial Inserts and Patellar ComponentsHowmedica Osteonics Corp. A.K.A. Stryker Orthopaedics K171365Arthrex Knee SystemsArthrex, Inc.

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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