meddevicedb.com FDA Device Reference

SWING-OFF SCREW

K130627 Class II Traditional
Decision Date
2013-08-21
Sponsor / Applicant
Advanced Interventional Technology, LLC

Technical Specification

510(k) Submission ID K130627
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2013-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SWING-OFF SCREW received FDA 510(k) clearance under submission number K130627, sponsored by Advanced Interventional Technology, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-08-21.

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.