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ORTHOPEDIC SALVAGE SYSTEM (OSS) 9CM COBALT - CHROME TIBIAL BODIES

K083827 Class II Special
Decision Date
2009-02-13
Sponsor / Applicant
Biomet Manufacturing Corp

Technical Specification

510(k) Submission ID K083827
Product Code KRO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3510
Decision Date 2009-02-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHOPEDIC SALVAGE SYSTEM (OSS) 9CM COBALT - CHROME TIBIAL BODIES received FDA 510(k) clearance under submission number K083827, sponsored by Biomet Manufacturing Corp. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2009-02-13.

Classification & Regulation

This clearance is catalogued under FDA product code KRO and 21 CFR 888.3510, within the Orthopedic review panel as a Class II device.