meddevicedb.com FDA Device Reference

POWER-LOAD COT FASTENER SYSTEM

K113598 Class II Traditional
Decision Date
2011-12-20
Sponsor / Applicant
Stryker Medical

Technical Specification

510(k) Submission ID K113598
Product Code FPO
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6910
Decision Date 2011-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWER-LOAD COT FASTENER SYSTEM received FDA 510(k) clearance under submission number K113598, sponsored by Stryker Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2011-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code FPO and 21 CFR 880.6910, within the General Hospital review panel as a Class II device.