meddevicedb.com FDA Device Reference

AOS TIBIAL NAIL

K070444 Class II Traditional
Decision Date
2007-06-14
Sponsor / Applicant
Advanced Orthopaedic Solutions, Inc.

Technical Specification

510(k) Submission ID K070444
Product Code HSB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3020
Decision Date 2007-06-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AOS TIBIAL NAIL received FDA 510(k) clearance under submission number K070444, sponsored by Advanced Orthopaedic Solutions, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2007-06-14.

Classification & Regulation

This clearance is catalogued under FDA product code HSB and 21 CFR 888.3020, within the Orthopedic review panel as a Class II device.