meddevicedb.com FDA Device Reference

ACETABULAR PLATES

K002941 Class II Traditional
Decision Date
2000-12-04
Sponsor / Applicant
Encore Orthopedics, Inc.

Technical Specification

510(k) Submission ID K002941
Product Code LWJ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 2000-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACETABULAR PLATES received FDA 510(k) clearance under submission number K002941, sponsored by Encore Orthopedics, 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 2000-12-04.

Classification & Regulation

This clearance is catalogued under FDA product code LWJ and 21 CFR 888.3360, within the Orthopedic review panel as a Class II device.