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PINNACLE CONSTRAINED ACETABULAR LINERS

K052079 Class II Traditional
Decision Date
2005-10-21
Sponsor / Applicant
DePuy Orthopaedics, Inc.

Technical Specification

510(k) Submission ID K052079
Product Code KWZ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3310
Decision Date 2005-10-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PINNACLE CONSTRAINED ACETABULAR LINERS received FDA 510(k) clearance under submission number K052079, sponsored by DePuy Orthopaedics, 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 2005-10-21.

Classification & Regulation

This clearance is catalogued under FDA product code KWZ and 21 CFR 888.3310, within the Orthopedic review panel as a Class II device.