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PS MEDICAL STRATA NSC LUMBOPERITONEAL VALVE AND SHUNT SYSTEM

K091312 Class II Traditional
Decision Date
2009-09-02
Sponsor / Applicant
Medtronic Neurosurgery

Technical Specification

510(k) Submission ID K091312
Product Code JXG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5550
Decision Date 2009-09-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PS MEDICAL STRATA NSC LUMBOPERITONEAL VALVE AND SHUNT SYSTEM received FDA 510(k) clearance under submission number K091312, sponsored by Medtronic Neurosurgery. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2009-09-02.

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.