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TOWNLEY TOTAL ELBOW SYSTEM

K955916 Class II Traditional
Decision Date
1996-08-08
Sponsor / Applicant
Biologically Oriented Prostheses

Technical Specification

510(k) Submission ID K955916
Product Code JDC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3150
Decision Date 1996-08-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOWNLEY TOTAL ELBOW SYSTEM received FDA 510(k) clearance under submission number K955916, sponsored by Biologically Oriented Prostheses. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1996-08-08.

Classification & Regulation

This clearance is catalogued under FDA product code JDC and 21 CFR 888.3150, within the Orthopedic review panel as a Class II device.