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FDA 510(k)

Physica Porous Femoral Components

K-Number: K243615 · 2024-12-18

ApplicantLima Corporate S.P.A.
Decision Date2024-12-18
Product CodeMBH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Physica Porous Femoral Components is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2024-12-18 under approval number K243615. 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 Porous Femoral Components?

Physica Porous Femoral Components is a medical device that received FDA 510(k) clearance on 2024-12-18. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K243615.

When was Physica Porous Femoral Components approved by the FDA?

Physica Porous Femoral Components received FDA 510(k) clearance on 2024-12-18, under approval number K243615.

What company makes Physica Porous Femoral Components?

Physica Porous Femoral Components is manufactured by Lima Corporate S.P.A..

What is the FDA product code for Physica Porous Femoral Components?

The FDA product code for Physica 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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