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DEPUY SUMMIT FX CEMENTED HIP PROSTHESIS

K023453 Class II Special
Decision Date
2002-11-13
Sponsor / Applicant
DePuy Orthopaedics, Inc.

Technical Specification

510(k) Submission ID K023453
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 2002-11-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DEPUY SUMMIT FX CEMENTED HIP PROSTHESIS received FDA 510(k) clearance under submission number K023453, sponsored by DePuy Orthopaedics, 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 2002-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.