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INTERMEDICS SELECT SHOULDER METAL-BACKED GLENOID

K884943 Class II Traditional
Decision Date
1989-04-27
Sponsor / Applicant
Intermedics Orthopedics

Technical Specification

510(k) Submission ID K884943
Product Code KWS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 1989-04-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTERMEDICS SELECT SHOULDER METAL-BACKED GLENOID received FDA 510(k) clearance under submission number K884943, sponsored by Intermedics Orthopedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1989-04-27.

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.