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BALANCED KNEE SYSTEM ULTRACONGRUENT TIBIAL INSERT

K090705 Class II Traditional
Decision Date
2009-10-09
Sponsor / Applicant
Ortho Development Corp.

Technical Specification

510(k) Submission ID K090705
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2009-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BALANCED KNEE SYSTEM ULTRACONGRUENT TIBIAL INSERT received FDA 510(k) clearance under submission number K090705, sponsored by Ortho Development 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 2009-10-09.

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.