meddevicedb.com FDA Device Reference

SBI AUTOFIX

K052576 Class II Traditional
Decision Date
2005-11-07
Sponsor / Applicant
Small Bone Innovations, LLC

Technical Specification

510(k) Submission ID K052576
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2005-11-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SBI AUTOFIX received FDA 510(k) clearance under submission number K052576, sponsored by Small Bone Innovations, 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 2005-11-07.

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.