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PALACOS R BONE CEMENT WITH GENTAMICIN

K030086 Class II Traditional
Decision Date
2003-12-17
Sponsor / Applicant
Biomet, Inc.

Technical Specification

510(k) Submission ID K030086
Product Code LOD
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3027
Decision Date 2003-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PALACOS R BONE CEMENT WITH GENTAMICIN received FDA 510(k) clearance under submission number K030086, sponsored by Biomet, 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 2003-12-17.

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.