meddevicedb.com FDA Device Reference

U2 ACETABULAR CUP, PLASMA SPRAY

K121777 Class II Special
Decision Date
2012-07-18
Sponsor / Applicant
United Orthopedic Corp.

Technical Specification

510(k) Submission ID K121777
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2012-07-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

U2 ACETABULAR CUP, PLASMA SPRAY received FDA 510(k) clearance under submission number K121777, sponsored by United Orthopedic Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-07-18.

Classification & Regulation

This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.