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EXACTECH POSTERIOR STABILIZED CEMENTED TOTAL KNEE SYSTEM

K933494 Class II Traditional
Decision Date
1995-03-10
Sponsor / Applicant
Exactech, Inc.

Technical Specification

510(k) Submission ID K933494
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 1995-03-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXACTECH POSTERIOR STABILIZED CEMENTED TOTAL KNEE SYSTEM received FDA 510(k) clearance under submission number K933494, sponsored by Exactech, 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 1995-03-10.

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.