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ASIAN INTRAMEDULLARY HIP SCREW NAILS

K050226 Class II Special
Decision Date
2005-02-11
Sponsor / Applicant
Smith & Nephew, Inc.

Technical Specification

510(k) Submission ID K050226
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2005-02-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASIAN INTRAMEDULLARY HIP SCREW NAILS received FDA 510(k) clearance under submission number K050226, sponsored by Smith & Nephew, 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 2005-02-11.

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.