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RAPID PROGRAMMER, VERSION 3.3.0

K091993 Class II Special
Decision Date
2009-07-31
Sponsor / Applicant
Advanced Neuromodulation Systems, Inc. (Ans Inc.)

Technical Specification

510(k) Submission ID K091993
Product Code GZB
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5880
Decision Date 2009-07-31
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RAPID PROGRAMMER, VERSION 3.3.0 received FDA 510(k) clearance under submission number K091993, sponsored by Advanced Neuromodulation Systems, Inc. (Ans Inc.). The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2009-07-31.

Classification & Regulation

This clearance is catalogued under FDA product code GZB and 21 CFR 882.5880, within the Neurology review panel as a Class II device.