meddevicedb.com FDA Device Reference

CONSERVE PLUS HA ACETABULAR SHELLS

K042530 Class III Special
Decision Date
2004-12-17
Sponsor / Applicant
Wrightmedicaltechnologyinc

Technical Specification

510(k) Submission ID K042530
Product Code KWA
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3330
Decision Date 2004-12-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONSERVE PLUS HA ACETABULAR SHELLS received FDA 510(k) clearance under submission number K042530, sponsored by Wrightmedicaltechnologyinc. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2004-12-17.

Classification & Regulation

This clearance is catalogued under FDA product code KWA and 21 CFR 888.3330, within the Orthopedic review panel as a Class III device.