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Evolve UniPolar Head

K143184 Class II Traditional
Decision Date
2015-03-17
Sponsor / Applicant
Signature Orthopaedics Pty, Ltd.

Technical Specification

510(k) Submission ID K143184
Product Code KWL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 2015-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Evolve UniPolar Head received FDA 510(k) clearance under submission number K143184, sponsored by Signature Orthopaedics Pty, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2015-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code KWL and 21 CFR 888.3360, within the Orthopedic review panel as a Class II device.