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OSTEONICS ELBOW PROSTHESIS

K861680 Class II Traditional
Decision Date
1986-06-27
Sponsor / Applicant
Osteonics Corp.

Technical Specification

510(k) Submission ID K861680
Product Code JDC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3150
Decision Date 1986-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEONICS ELBOW PROSTHESIS received FDA 510(k) clearance under submission number K861680, sponsored by Osteonics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1986-06-27.

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.