meddevicedb.com FDA Device Reference

PINNACLETM Constrained Acetabular Liners

K240639 Class II Special
Decision Date
2024-04-04
Sponsor / Applicant
Depuy Ireland UC

Technical Specification

510(k) Submission ID K240639
Product Code KWZ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3310
Decision Date 2024-04-04
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PINNACLETM Constrained Acetabular Liners received FDA 510(k) clearance under submission number K240639, sponsored by Depuy Ireland UC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-04-04.

Classification & Regulation

This clearance is catalogued under FDA product code KWZ and 21 CFR 888.3310, within the Orthopedic review panel as a Class II device.