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MECTACER BIOLOX(R) DELTA FEMORAL HEADS

K112115 Class II Special
Decision Date
2011-10-07
Sponsor / Applicant
Medacta International

Technical Specification

510(k) Submission ID K112115
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 2011-10-07
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MECTACER BIOLOX(R) DELTA FEMORAL HEADS received FDA 510(k) clearance under submission number K112115, sponsored by Medacta International. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-10-07.

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.