meddevicedb.com FDA Device Reference

ACE AIM TTC FUSION NAIL

K003797 Class II Special
Decision Date
2000-12-15
Sponsor / Applicant
DePuy Orthopaedics, Inc.

Technical Specification

510(k) Submission ID K003797
Product Code HSB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3020
Decision Date 2000-12-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACE AIM TTC FUSION NAIL received FDA 510(k) clearance under submission number K003797, sponsored by DePuy Orthopaedics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2000-12-15.

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.