meddevicedb.com FDA Device Reference

FPC/SFPC/RFPC ACETABULAR COMPONENT

K915529 Class III Traditional
Decision Date
1993-07-13
Sponsor / Applicant
Implantology Corp.

Technical Specification

510(k) Submission ID K915529
Product Code JDL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3320
Decision Date 1993-07-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FPC/SFPC/RFPC ACETABULAR COMPONENT received FDA 510(k) clearance under submission number K915529, sponsored by Implantology 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 1993-07-13.

Classification & Regulation

This clearance is catalogued under FDA product code JDL and 21 CFR 888.3320, within the Orthopedic review panel as a Class III device.