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FRAGMENT PLATE SYSTEM, SCREWS, PINS AND K-WIRES

K041081 Class II Traditional
Decision Date
2004-07-01
Sponsor / Applicant
Hand Innovations, Inc.

Technical Specification

510(k) Submission ID K041081
Product Code KTT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2004-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FRAGMENT PLATE SYSTEM, SCREWS, PINS AND K-WIRES received FDA 510(k) clearance under submission number K041081, sponsored by Hand Innovations, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2004-07-01.

Classification & Regulation

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