meddevicedb.com FDA Device Reference

MULTIDIRECTIONAL THREADED PEG

K060864 Class II Special
Decision Date
2006-04-28
Sponsor / Applicant
Hand Innovations, LLC

Technical Specification

510(k) Submission ID K060864
Product Code LXT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2006-04-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTIDIRECTIONAL THREADED PEG received FDA 510(k) clearance under submission number K060864, sponsored by Hand Innovations, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-04-28.

Classification & Regulation

This clearance is catalogued under FDA product code LXT and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.