Medical Device Manufacturer · US , Plano , TX

Advanced Neuromodulation Systems - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1999

Total

Cleared

Denied

Advanced Neuromodulation Systems has 25 FDA 510(k) cleared neurology devices. Based in Plano, US.

Historical record: 25 cleared submissions from 1999 to 2009.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Advanced Neuromodulation Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Advanced Neuromodulation Systems

25 devices

1-25 of 25

Cleared Dec 23, 2009

SWIFT-LOCK ANCHOR, MODEL 1192

K092371 · GZB

Neurology · 140d

Cleared Jun 02, 2009

PENTA LEAD KITS, MODELS: 3227-3234

K090907 · GZB

Neurology · 62d

Cleared Jul 18, 2008

CINCH ANCHOR, MODEL 1194

K081208 · GZB

Neurology · 80d

Cleared Oct 11, 2007

WIDE SPACED QUATTRODE LEADS

TRIPOLE 8C AND 16C AND EXCLAIM 8 LAMITRODE SERIES LEADS

K063080 · GZB

Neurology · 63d

Cleared Dec 15, 2005

ANS 90 CM AND 110 CM (3100 AND 3200 SERIES) LEAD KIT

AXXESS BUTTERFLY ANCHOR

K052418 · GZB

Neurology · 24d

Cleared May 18, 2005

ANS SCS ACCESSORY KIT

K050922 · GZB

Neurology · 35d

Cleared Apr 21, 2005

TRIAL CABLE RETENTION CLIP

MTS MULTIPROGRAM TRIAL STIMULATOR SYSTEM

K033757 · GZB

Neurology · 60d

Cleared Dec 04, 2003

LAMITRODE SPINAL CORD STIMULATION LEADS

K033429 · GZB

Neurology · 37d

Cleared Oct 06, 2003

MODIFICATION TO RENEW LEAD EXTENSION

K032751 · GZB

Neurology · 31d

Cleared Oct 03, 2003

ANS AXXESS PERCUTANEOUS LEAD

MODIFICATION TO AXXESS SPINAL CORD STIMULATION LEAD

RENEW NEUROSTIMULATION SYSTEM

Advanced Neuromodulation Systems - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Advanced Neuromodulation Systems

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