meddevicedb.com FDA Device Reference

ORTHO SOLUTIONS TRAUMA IMPLANTS FOR OSTEOSYNTHESIS

K110895 Class II Traditional
Decision Date
2011-12-19
Sponsor / Applicant
Ortho Solutions Limited

Technical Specification

510(k) Submission ID K110895
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2011-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHO SOLUTIONS TRAUMA IMPLANTS FOR OSTEOSYNTHESIS received FDA 510(k) clearance under submission number K110895, 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 2011-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.