Advanced Neuromodulation Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Neuromodulation Systems - FDA 510(k) Cleared Devices
Recent clearances: SWIFT-LOCK ANCHOR, MODEL 1192, PENTA LEAD KITS, MODELS: 3227-3234, CINCH ANCHOR, MODEL 1194
25
Total
25
Cleared
0
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.
FDA 510(k) Regulatory Record - Advanced Neuromodulation Systems
25 devices
Cleared
Dec 23, 2009
SWIFT-LOCK ANCHOR, MODEL 1192
Neurology
140d
Cleared
Jun 02, 2009
PENTA LEAD KITS, MODELS: 3227-3234
Neurology
62d
Cleared
Jul 18, 2008
CINCH ANCHOR, MODEL 1194
Neurology
80d
Cleared
Oct 11, 2007
WIDE SPACED QUATTRODE LEADS
Neurology
41d
Cleared
Apr 11, 2007
TRIAL CABLE, 3009
Neurology
14d
Cleared
Dec 12, 2006
TRIPOLE 8C AND 16C AND EXCLAIM 8 LAMITRODE SERIES LEADS
Neurology
63d
Cleared
Dec 15, 2005
ANS 90 CM AND 110 CM (3100 AND 3200 SERIES) LEAD KIT
Neurology
24d
Cleared
Nov 22, 2005
RAPID PROGEAMMER 3.0
Neurology
84d
Cleared
Sep 26, 2005
AXXESS BUTTERFLY ANCHOR
Neurology
24d
Cleared
May 18, 2005
ANS SCS ACCESSORY KIT
Neurology
35d
Cleared
Apr 21, 2005
TRIAL CABLE RETENTION CLIP
Neurology
41d
Cleared
Mar 25, 2004
RAPID PROGRAMMER
Neurology
17d