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APR REVISION HIP PROSTHESIS, FEMORAL COMPONENT

K853524 Class II Traditional
Decision Date
1985-11-22
Sponsor / Applicant
Intermedics Orthopedics

Technical Specification

510(k) Submission ID K853524
Product Code KMC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3340
Decision Date 1985-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APR REVISION HIP PROSTHESIS, FEMORAL COMPONENT received FDA 510(k) clearance under submission number K853524, 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 1985-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code KMC and 21 CFR 888.3340, within the Orthopedic review panel as a Class II device.