meddevicedb.com FDA Device Reference

Extended HA Half Pins

K210784 Class II Special
Decision Date
2021-04-02
Sponsor / Applicant
Smith & Nephew, Inc.

Technical Specification

510(k) Submission ID K210784
Product Code JDW
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2021-04-02
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Extended HA Half Pins received FDA 510(k) clearance under submission number K210784, 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 2021-04-02.

Classification & Regulation

This clearance is catalogued under FDA product code JDW and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.