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PARADIS VASO SHIELD

K090022 Class II Traditional
Decision Date
2009-04-20
Sponsor / Applicant
Spinemedica, LLC

Technical Specification

510(k) Submission ID K090022
Product Code OMR
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3470
Decision Date 2009-04-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PARADIS VASO SHIELD received FDA 510(k) clearance under submission number K090022, sponsored by Spinemedica, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2009-04-20.

Classification & Regulation

This clearance is catalogued under FDA product code OMR and 21 CFR 870.3470, within the Cardiovascular review panel as a Class II device.