meddevicedb.com FDA Device Reference

OSTEONICS RESTORATION MONOLITHIC HIP STEM

K943774 Class II Traditional
Decision Date
1995-03-06
Sponsor / Applicant
Osteonics Corp.

Technical Specification

510(k) Submission ID K943774
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 1995-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEONICS RESTORATION MONOLITHIC HIP STEM received FDA 510(k) clearance under submission number K943774, sponsored by Osteonics 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 1995-03-06.

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.