meddevicedb.com FDA Device Reference

Quick-Start Orthopaedic Fixation Screw and Reverse Thread Screw

K231819 Class II Traditional
Decision Date
2023-09-05
Sponsor / Applicant
Innovate Orthopaedics Limited

Technical Specification

510(k) Submission ID K231819
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2023-09-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Quick-Start Orthopaedic Fixation Screw and Reverse Thread Screw received FDA 510(k) clearance under submission number K231819, sponsored by Innovate Orthopaedics Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-09-05.

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.