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METAL TRANSCEND ARTICULATION SYSTEM

K004043 Class III Abbreviated
Decision Date
2001-07-13
Sponsor / Applicant
Wrightmedicaltechnologyinc

Technical Specification

510(k) Submission ID K004043
Product Code JDL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3320
Decision Date 2001-07-13
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

METAL TRANSCEND ARTICULATION SYSTEM received FDA 510(k) clearance under submission number K004043, sponsored by Wrightmedicaltechnologyinc. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2001-07-13.

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.