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EXPRT™ Revision Hip System - EXPRT™ Hip Distal Stem, EXPRT™ Hip Standard Offset Proximal Body Implant, EXPRT™ Hip Lateral Offset Proximal Body Implant, EXPRT™ Hip Capture Bolt

K163497 Class II Traditional
Decision Date
2017-03-02
Sponsor / Applicant
Encore Medical L.P.

Technical Specification

510(k) Submission ID K163497
Product Code KWZ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3310
Decision Date 2017-03-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXPRT™ Revision Hip System - EXPRT™ Hip Distal Stem, EXPRT™ Hip Standard Offset Proximal Body Implant, EXPRT™ Hip Lateral Offset Proximal Body Implant, EXPRT™ Hip Capture Bolt received FDA 510(k) clearance under submission number K163497, sponsored by Encore Medical L.P.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-03-02.

Classification & Regulation

This clearance is catalogued under FDA product code KWZ and 21 CFR 888.3310, within the Orthopedic review panel as a Class II device.