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Klassic Knee System-Sombrero Patella

K150105 Class II Special
Decision Date
2015-02-17
Sponsor / Applicant
Total Joint Orthopedics, Inc.

Technical Specification

510(k) Submission ID K150105
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2015-02-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Klassic Knee System-Sombrero Patella received FDA 510(k) clearance under submission number K150105, sponsored by Total Joint Orthopedics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2015-02-17.

Classification & Regulation

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