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Continuum and Trilogy Integrated Taper (IT) Acetabular Systems

K151448 Class II Traditional
Decision Date
2015-08-13
Sponsor / Applicant
Zimmer, Inc.

Technical Specification

510(k) Submission ID K151448
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2015-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Continuum and Trilogy Integrated Taper (IT) Acetabular Systems received FDA 510(k) clearance under submission number K151448, 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 2015-08-13.

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.