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PATIENT MATCHED HIP STEM

K053246 Class II Abbreviated
Decision Date
2006-07-12
Sponsor / Applicant
Smith & Nephew, Inc.

Technical Specification

510(k) Submission ID K053246
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 2006-07-12
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATIENT MATCHED HIP STEM received FDA 510(k) clearance under submission number K053246, 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 2006-07-12.

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.