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OSTEONICS(R) 6011 HIP STEM SERIES

K905158 Class II Traditional
Decision Date
1991-01-04
Sponsor / Applicant
Osteonics Corp.

Technical Specification

510(k) Submission ID K905158
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 1991-01-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEONICS(R) 6011 HIP STEM SERIES received FDA 510(k) clearance under submission number K905158, 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 1991-01-04.

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.