Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by PENNY HOUSTON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070847
03/28/2007
TRIAL CABLE, 3009
ADVANCED NEUROMODULATION SYSTEMS
K081208
04/29/2008
CINCH ANCHOR, MODEL 1194
ADVANCED NEUROMODULATION SYSTEMS
K112214
08/02/2011
OCTRODEX(TM), QUATTRODEX(TM), INTRODEX(TM), EPIDURAL NEEDLE, STYLETS
ST. JUDE MEDICAL NEUROMODULATION
K092371
08/05/2009
SWIFT-LOCK ANCHOR, MODEL 1192
ADVANCED NEUROMODULATION SYSTEMS
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact