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J-SERIES OMEGA TOTAL HIP SYSTEM

K990003 Class II Traditional
Decision Date
1999-02-24
Sponsor / Applicant
Osteoimplant Technology, Inc.

Technical Specification

510(k) Submission ID K990003
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 1999-02-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

J-SERIES OMEGA TOTAL HIP SYSTEM received FDA 510(k) clearance under submission number K990003, sponsored by Osteoimplant Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1999-02-24.

Classification & Regulation

This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.