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CI../..X liner for NOVAE Dual Mobility Acetabular Cup

K142675 Class II Traditional
Decision Date
2015-01-15
Sponsor / Applicant
Serf

Technical Specification

510(k) Submission ID K142675
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 2015-01-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CI../..X liner for NOVAE Dual Mobility Acetabular Cup received FDA 510(k) clearance under submission number K142675, sponsored by Serf. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2015-01-15.

Classification & Regulation

This clearance is catalogued under FDA product code LZO and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.