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ORTHO SOLUTIONS TRAUMA PLATES FOR OSTEOSYSNTHESIS

K120360 Class II Traditional
Decision Date
2012-05-29
Sponsor / Applicant
Ortho Solutions Limited

Technical Specification

510(k) Submission ID K120360
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2012-05-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHO SOLUTIONS TRAUMA PLATES FOR OSTEOSYSNTHESIS received FDA 510(k) clearance under submission number K120360, sponsored by Ortho Solutions Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-05-29.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.