meddevicedb.com FDA Device Reference

T2 FEMORAL NAIL

K081152 Class II Special
Decision Date
2008-06-10
Sponsor / Applicant
Howmedica Osteonics Corp.

Technical Specification

510(k) Submission ID K081152
Product Code HSB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3020
Decision Date 2008-06-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

T2 FEMORAL NAIL received FDA 510(k) clearance under submission number K081152, sponsored by Howmedica Osteonics Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2008-06-10.

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.