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Advanced Neuromodulation Systems Inc.

9 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Advanced Neuromodulation Systems, Brio DBS System implantable neurostimulator, IPG or R-IP recall (Z-0894-2013)Advanced Neuromodulation Systems Inc.2013-02-28
The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel, rechargeable, multi-progra recall (Z-0025-2013)Advanced Neuromodulation Systems Inc.2012-10-09
Eon (Model 3716) IPG is a dual channel; 8-contact receiver designed to be connected to 4, recall (Z-2280-2012)Advanced Neuromodulation Systems Inc.2012-08-28
The Eon Mini Neurostimulation (IPG) System (Model 3788) is a 16-channel, rechargeable, mul recall (Z-2281-2012)Advanced Neuromodulation Systems Inc.2012-08-28
Eon Mini Neurostimulation (IPG) System (Model 3788); The product is indicated as an aid in recall (Z-1983-2012)Advanced Neuromodulation Systems Inc.2012-07-10
Eon Mini Neurostimulation (IPG) System Model 3788 System is indicated as an aid in the man recall (Z-2607-2011)Advanced Neuromodulation Systems Inc.2011-06-22
Eon Mini Implantable Pulse Generator (IPG). Advanced Neuromodulation Systems, Inc. Plano, recall (Z-1599-2010)Advanced Neuromodulation Systems, Inc2010-05-13
Swift-Lock (TM) Anchor Accessory Kit, Directions For Use Model 1192, ANS, A St. Jude Medic recall (Z-1425-2010)Advanced Neuromodulation Systems, Inc2010-04-21
Eon Rechargeable Implantable Pulse Generator (IPG) System recall (Z-0170-2010)Advanced Neuromodulation Systems, Inc2009-11-10

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Every clearance here is in the API, with alerts when new ones post.