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SMITH & NEPHEW, INC. JOURNEY SELECT KNEE SYSTEM

K093056 Class II Traditional
Decision Date
2009-12-15
Sponsor / Applicant
Smith & Nephew, Inc.

Technical Specification

510(k) Submission ID K093056
Product Code NPJ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2009-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMITH & NEPHEW, INC. JOURNEY SELECT KNEE SYSTEM received FDA 510(k) clearance under submission number K093056, sponsored by Smith & Nephew, 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 2009-12-15.

Classification & Regulation

This clearance is catalogued under FDA product code NPJ and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.