meddevicedb.com FDA Device Reference

RIM-FIX, ACETABULAR CUP

K993713 Class II Traditional
Decision Date
2000-01-28
Sponsor / Applicant
Surgical Implants, Inc.

Technical Specification

510(k) Submission ID K993713
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 2000-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RIM-FIX, ACETABULAR CUP received FDA 510(k) clearance under submission number K993713, sponsored by Surgical Implants, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2000-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.