meddevicedb.com FDA Device Reference

SIGN Compression Screw System

K153759 Class II Traditional
Decision Date
2016-02-25
Sponsor / Applicant
Sign Fracture Care International

Technical Specification

510(k) Submission ID K153759
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2016-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIGN Compression Screw System received FDA 510(k) clearance under submission number K153759, sponsored by Sign Fracture Care International. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2016-02-25.

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.