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OSTEONICS OMNIFIT FORGED HIP STEM SERIES

K933561 Class II Traditional
Decision Date
1994-03-09
Sponsor / Applicant
Osteonics Corp.

Technical Specification

510(k) Submission ID K933561
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 1994-03-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEONICS OMNIFIT FORGED HIP STEM SERIES received FDA 510(k) clearance under submission number K933561, 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 1994-03-09.

Classification & Regulation

This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.