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Physica Porous Femoral Components

K243615 Class II Special
Decision Date
2024-12-18
Sponsor / Applicant
Lima Corporate S.P.A.

Technical Specification

510(k) Submission ID K243615
Product Code MBH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3565
Decision Date 2024-12-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Physica Porous Femoral Components received FDA 510(k) clearance under submission number K243615, sponsored by Lima Corporate S.P.A.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-12-18.

Classification & Regulation

This clearance is catalogued under FDA product code MBH and 21 CFR 888.3565, within the Orthopedic review panel as a Class II device.