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X-SERIES BI-METRIC HIP FEMORAL COMPONENTS

K020580 Class II Special
Decision Date
2002-03-22
Sponsor / Applicant
Biomet, Inc.

Technical Specification

510(k) Submission ID K020580
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2002-03-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X-SERIES BI-METRIC HIP FEMORAL COMPONENTS received FDA 510(k) clearance under submission number K020580, sponsored by Biomet, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2002-03-22.

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.