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FIRST CHOICE DRUJ SYSTEM, PARTIAL HEAD IMPLANT

K112481 Class II Traditional
Decision Date
2012-04-09
Sponsor / Applicant
Ascension Orthopedic

Technical Specification

510(k) Submission ID K112481
Product Code KXE
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3810
Decision Date 2012-04-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FIRST CHOICE DRUJ SYSTEM, PARTIAL HEAD IMPLANT received FDA 510(k) clearance under submission number K112481, sponsored by Ascension Orthopedic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-04-09.

Classification & Regulation

This clearance is catalogued under FDA product code KXE and 21 CFR 888.3810, within the Orthopedic review panel as a Class II device.