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SMARTSET GMV ENDURANCE GENTAMICIN BONE CEMENT

K033382 Class II Traditional
Decision Date
2004-02-05
Sponsor / Applicant
DePuy Orthopaedics, Inc.

Technical Specification

510(k) Submission ID K033382
Product Code LOD
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3027
Decision Date 2004-02-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMARTSET GMV ENDURANCE GENTAMICIN BONE CEMENT received FDA 510(k) clearance under submission number K033382, 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 2004-02-05.

Classification & Regulation

This clearance is catalogued under FDA product code LOD and 21 CFR 888.3027, within the Orthopedic review panel as a Class II device.