Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by HEATHER GUERIN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100089
01/12/2010
SYNTHES T-PAL SPACER
SYNTHES SPINE
K120275
01/30/2012
SYNTHES ACIS/VERTEBRAL SPACER CR
SYNTHES (USA) LLC
K120838
03/20/2012
SYNTHES MATRIX SYSTEM
SYNTHES SPINE
K120928
03/27/2012
SYNTHES MATRIX SYSTEM
SYNTHES SPINE
K111048
04/15/2011
SYNTHES SCOUT TACK FIXATION
SYNTHES SPINE
K111358
05/16/2011
SYNTHES USS
SYNTHES SPINE
K131792
06/18/2013
SYNTHECEL DURA REPAIR, SYNTHECEL DURA ONLAY
SYNTHES INC
K113044
10/12/2011
SYNTHES MIRS
SYNTHES SPINE
K113149
10/24/2011
SYNTHES USS CONNECTORS
SYNTHES SPINE
K103320
11/12/2010
SYNTHES XRL
SYNTHES SPINE CO.LP
K093668
11/27/2009
SYNTHES MATRIX MIS RODS
SYNTHES (USA)
K103558
12/02/2010
SYNTHES SCOUT VESSEL GUARD
SYNTHES SPINE
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact