meddevicedb.com FDA Device Reference

OSV II LOW FLOW LOW PRO VALVE

K093968 Class II Special
Decision Date
2010-01-22
Sponsor / Applicant
Integra LifeSciences Corporation

Technical Specification

510(k) Submission ID K093968
Product Code JXG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5550
Decision Date 2010-01-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSV II LOW FLOW LOW PRO VALVE received FDA 510(k) clearance under submission number K093968, sponsored by Integra LifeSciences Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2010-01-22.

Classification & Regulation

This clearance is catalogued under FDA product code JXG and 21 CFR 882.5550, within the Neurology review panel as a Class II device.