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MONOBLOCK PRESS-FIT HIP STEM

K060072 Class II Traditional
Decision Date
2006-08-24
Sponsor / Applicant
Omni Life Science, Inc.

Technical Specification

510(k) Submission ID K060072
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2006-08-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MONOBLOCK PRESS-FIT HIP STEM received FDA 510(k) clearance under submission number K060072, sponsored by Omni Life Science, 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 2006-08-24.

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.