meddevicedb.com FDA Device Reference

CHARLOTTE CAROLINA JONES FRACTURE SYSTEM SCREW

K140952 Class II Special
Decision Date
2014-05-15
Sponsor / Applicant
Wrightmedicaltechnologyinc

Technical Specification

510(k) Submission ID K140952
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2014-05-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHARLOTTE CAROLINA JONES FRACTURE SYSTEM SCREW received FDA 510(k) clearance under submission number K140952, sponsored by Wrightmedicaltechnologyinc. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2014-05-15.

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.