meddevicedb.com FDA Device Reference

SBI WRISTFIT

K051747 Class II Traditional
Decision Date
2005-09-06
Sponsor / Applicant
Small Bone Innovations, LLC

Technical Specification

510(k) Submission ID K051747
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2005-09-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SBI WRISTFIT received FDA 510(k) clearance under submission number K051747, 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 2005-09-06.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.