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MODIFICATION OF ENCORE LINEAR POROUS COATED HIP

K991325 Class II Traditional
Decision Date
1999-06-25
Sponsor / Applicant
Encore Orthopedics, Inc.

Technical Specification

510(k) Submission ID K991325
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 1999-06-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION OF ENCORE LINEAR POROUS COATED HIP received FDA 510(k) clearance under submission number K991325, sponsored by Encore Orthopedics, 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 1999-06-25.

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.