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CONSERVE TOTAL FEMORAL HEAD

K051348 Class III Traditional
Decision Date
2005-08-19
Sponsor / Applicant
Wrightmedicaltechnologyinc

Technical Specification

510(k) Submission ID K051348
Product Code JDL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3320
Decision Date 2005-08-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONSERVE TOTAL FEMORAL HEAD received FDA 510(k) clearance under submission number K051348, sponsored by Wrightmedicaltechnologyinc. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2005-08-19.

Classification & Regulation

This clearance is catalogued under FDA product code JDL and 21 CFR 888.3320, within the Orthopedic review panel as a Class III device.