meddevicedb.com FDA Device Reference

ZCA All-Poly Acetabular Cups

K191449 Class II Traditional
Decision Date
2020-07-16
Sponsor / Applicant
Zimmer, Inc.

Technical Specification

510(k) Submission ID K191449
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 2020-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZCA All-Poly Acetabular Cups received FDA 510(k) clearance under submission number K191449, sponsored by Zimmer, 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 2020-07-16.

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.