meddevicedb.com FDA Device Reference

OSTEONICS SHOULDER PROSTHESIS

K862535 Class II Traditional
Decision Date
1986-09-02
Sponsor / Applicant
Osteonics Corp.

Technical Specification

510(k) Submission ID K862535
Product Code KWS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 1986-09-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEONICS SHOULDER PROSTHESIS received FDA 510(k) clearance under submission number K862535, 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 1986-09-02.

Classification & Regulation

This clearance is catalogued under FDA product code KWS and 21 CFR 888.3660, within the Orthopedic review panel as a Class II device.