meddevicedb.com FDA Device Reference

TRABECULAR METAL FEMORAL CONE AUGMENTS

K103517 Class II Traditional
Decision Date
2011-02-15
Sponsor / Applicant
Zimmer Trabecular Metal Technology, Inc.

Technical Specification

510(k) Submission ID K103517
Product Code MBH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3565
Decision Date 2011-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRABECULAR METAL FEMORAL CONE AUGMENTS received FDA 510(k) clearance under submission number K103517, sponsored by Zimmer Trabecular Metal Technology, 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 2011-02-15.

Classification & Regulation

This clearance is catalogued under FDA product code MBH and 21 CFR 888.3565, within the Orthopedic review panel as a Class II device.