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LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE

K896850 Class II Traditional
Decision Date
1990-06-05
Sponsor / Applicant
Lima Intl. Corp.

Technical Specification

510(k) Submission ID K896850
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 1990-06-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE received FDA 510(k) clearance under submission number K896850, sponsored by Lima Intl. Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1990-06-05.

Classification & Regulation

This clearance is catalogued under FDA product code LZO and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.