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E-POLY TIBIAL BEARINGS

K080528 Class II Traditional
Decision Date
2008-06-17
Sponsor / Applicant
Biomet Orthopedics, Inc.

Technical Specification

510(k) Submission ID K080528
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2008-06-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

E-POLY TIBIAL BEARINGS received FDA 510(k) clearance under submission number K080528, sponsored by Biomet Orthopedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2008-06-17.

Classification & Regulation

This clearance is catalogued under FDA product code JWH and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.