meddevicedb.com FDA Device Reference

NATURAL-KNEE SYSTEM SYSTEM W/COCR/CSTI(TM)

K902335 Class II Traditional
Decision Date
1990-08-22
Sponsor / Applicant
Intermedics Orthopedics

Technical Specification

510(k) Submission ID K902335
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 1990-08-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NATURAL-KNEE SYSTEM SYSTEM W/COCR/CSTI(TM) received FDA 510(k) clearance under submission number K902335, 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 1990-08-22.

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.