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EMPOWR Stem Extender, 50mm

K230441 Class II Special
Decision Date
2023-03-17
Sponsor / Applicant
Encore Medical, L.P Dba Enovis

Technical Specification

510(k) Submission ID K230441
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2023-03-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMPOWR Stem Extender, 50mm received FDA 510(k) clearance under submission number K230441, sponsored by Encore Medical, L.P Dba Enovis. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code JWH and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.