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GMK Revision & Hinge Extension - TiNbN Coating

K210010 Class II Traditional
Decision Date
2021-03-02
Sponsor / Applicant
Medacta International S.A.

Technical Specification

510(k) Submission ID K210010
Product Code KRO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3510
Decision Date 2021-03-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GMK Revision & Hinge Extension - TiNbN Coating received FDA 510(k) clearance under submission number K210010, sponsored by Medacta International S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2021-03-02.

Classification & Regulation

This clearance is catalogued under FDA product code KRO and 21 CFR 888.3510, within the Orthopedic review panel as a Class II device.