Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by SEVRINA CIUCCI
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090815
03/25/2009
PERCUTANEOUS DISCECTOMY SYSTEM
LAURIMED LLC
K040832
03/31/2004
C-PORT ANASTOMOSIS SYSTEM (DEPLOYMENT SYSTEM, CLIP, ACCESSORIES), MODEL FG-000050
CARDICA, INC.
K021062
04/02/2002
CHITO-SEAL
ABBOTT VASCULAR INC.
K091818
06/18/2009
LAURIMED SPINAL INJECTION SYSTEM
LAURIMED LLC
K072261
08/14/2007
FINESSE SYSTEM
PRIMAEVA MEDICAL, INC.
K112579
09/06/2011
WILDCAT 5F GUIDEWIRE SUPPORT CATHETER
AVINGER, INC.
K113362
11/15/2011
SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS)
SPINE VIEW, INC.
K014118
12/14/2001
MODIFICATION TO SUPERCROSS CATHETER
ABBOTT VASCULAR INC.
K093866
12/17/2009
EVALVE STEERABLE GUIDE CATHETER
EVALVE INC
K113838
12/28/2011
WILDCAT CATHETER
AVINGER, INC.
K083909
12/30/2008
SPINAL INJECTION SYSTEM
LAURIMED LLC
K111704
06/17/2011
AVINGER WILDCAT 6F GUIDEWIRE SUPPORT CATHETER AND JUICEBOX
AVINGER, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact