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SIMPLEX P SPEEDSET BONE CEMENT

K053198 Class II Traditional
Decision Date
2006-01-26
Sponsor / Applicant
Howmedica Osteonics Corp.

Technical Specification

510(k) Submission ID K053198
Product Code LOD
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3027
Decision Date 2006-01-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIMPLEX P SPEEDSET BONE CEMENT received FDA 510(k) clearance under submission number K053198, sponsored by Howmedica Osteonics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-01-26.

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.