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SMITH & NEPHEW HIP SYSTEMS WITH HA

K090982 Class II Abbreviated
Decision Date
2010-04-21
Sponsor / Applicant
Smith & Nephew, Inc.

Technical Specification

510(k) Submission ID K090982
Product Code MEH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 2010-04-21
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMITH & NEPHEW HIP SYSTEMS WITH HA received FDA 510(k) clearance under submission number K090982, sponsored by Smith & Nephew, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2010-04-21.

Classification & Regulation

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