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FDA 510(k) Applications Submitted by Katryna Warren
FDA 510(k) Number
Submission Date
Device Name
Applicant
K991784
05/25/1999
RENEW LEAD EXTENSION
ADVANCED NEUROMODULATION SYSTEMS
K032349
06/30/2003
PLACER
ADVANCED NEUROMODULATION SYSTEMS
K032034
07/01/2003
ANS AXXESS PERCUTANEOUS LEAD
ADVANCED NEUROMODULATION SYSTEMS
K191795
07/03/2019
AOCup Lens Case with AODisc
Alcon Laboratories, Inc.
K022222
07/09/2002
LAMITRODE S-SERIES (S4 AND S8) LEADS
ADVANCED NEUROMODULATION SYSTEM,INC
K052374
08/30/2005
RAPID PROGEAMMER 3.0
ADVANCED NEUROMODULATION SYSTEMS
K992946
09/01/1999
RENEW RECEIVER
ADVANCED NEUROMODULATION SYSTEMS
K173538
11/15/2017
Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODisc
Alcon Laboratories, Inc.
K033757
12/01/2003
MTS MULTIPROGRAM TRIAL STIMULATOR SYSTEM
ADVANCED NEUROMODULATION SYSTEMS
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