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APR OVERSIZED HIP STEM

K961921 Class II Traditional
Decision Date
1996-08-05
Sponsor / Applicant
Intermedics Orthopedics

Technical Specification

510(k) Submission ID K961921
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 1996-08-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APR OVERSIZED HIP STEM received FDA 510(k) clearance under submission number K961921, 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 1996-08-05.

Classification & Regulation

This clearance is catalogued under FDA product code LZO and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.