meddevicedb.com FDA Device Reference

ALEXIS O WOUND PROTECTOR/RETRACTOR

K113268 Class II Traditional
Decision Date
2013-02-08
Sponsor / Applicant
Applied Medical Resources Corp.

Technical Specification

510(k) Submission ID K113268
Product Code KGW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2013-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALEXIS O WOUND PROTECTOR/RETRACTOR received FDA 510(k) clearance under submission number K113268, sponsored by Applied Medical Resources Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2013-02-08.

Classification & Regulation

This clearance is catalogued under FDA product code KGW and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.