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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 the device name listed in this FDA 510(k) record. The listed applicant is Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2025-05-22 under 510(k) 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. The listed applicant is Lima Corporate S.P.A.. The 510(k) number is K250980.

When did Physica System (Physica CR Porous Femoral components) receive FDA 510(k) clearance?

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

Who is the listed applicant for Physica System (Physica CR Porous Femoral components)?

The FDA 510(k) record lists Lima Corporate S.P.A. as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Lima Corporate S.P.A. as applicant

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.

K252352SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral SystemK251718ArTT Augments and Buttresses and Bone ScrewsK243826SMR Reverse HP Shoulder SystemK243615Physica Porous Femoral ComponentsK234011AMF TT ConesK233712PRIMA Humeral System; PRIMA TT Glenoid

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Related Devices (Code: MBH)

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.

K251840Zimmer® Persona® Personalized Knee SystemZimmer, Inc.K253189Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs)Zimmer, Inc.K253328GMK 3D Metal Tibial Tray ExtensionMedacta International S.A.K253637Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing InsertHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK253239Active-V Total Knee System; World Total Knee SystemSignature Orthopaedics Pty, Ltd.K253161Balanced Knee System TriMax Porous Femoral ComponentsOrtho Development Corp.

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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