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PATELLOFEMORAL JOINT PROSTHESIS

K962190 Class II Traditional
Decision Date
1996-10-28
Sponsor / Applicant
Intermedics Orthopedics

Technical Specification

510(k) Submission ID K962190
Product Code KRR
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3540
Decision Date 1996-10-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATELLOFEMORAL JOINT PROSTHESIS received FDA 510(k) clearance under submission number K962190, sponsored by Intermedics Orthopedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1996-10-28.

Classification & Regulation

This clearance is catalogued under FDA product code KRR and 21 CFR 888.3540, within the Orthopedic review panel as a Class II device.