meddevicedb.com FDA Device Reference

SimpliFix Hip System

K230053 Class II Traditional
Decision Date
2023-04-19
Sponsor / Applicant
Stabiliz Orthopaedics, Inc.

Technical Specification

510(k) Submission ID K230053
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2023-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SimpliFix Hip System received FDA 510(k) clearance under submission number K230053, sponsored by Stabiliz Orthopaedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.