Kfx Medical - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Kfx Medical has 7 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Historical record: 7 cleared submissions from 2006 to 2012. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kfx Medical Filter by specialty or product code using the sidebar.
7 devices
Cleared
Jun 07, 2012
APPIANFX SUTURE ANCHOR (6MM) (5MM) APPIANFX TISSUE ANCHOR
Orthopedic
79d
Cleared
May 20, 2010
KFX APPIANFX PEEK FEMORAL IMPLANT WITH INSERTER
Orthopedic
23d
Cleared
Mar 06, 2009
KFX PEEK BONE ANCHOR WITH PRE-ATTACHED SUTURES AND INSERTER HANDLE
Orthopedic
88d
Cleared
Jul 03, 2008
SUTURE LOCK NAIL BONE ANCHOR WITH WHITE (KFX-W-200) & BLUE (KFX-B-200)...
Orthopedic
27d
Cleared
Feb 29, 2008
5.5 MM SUTURE LOCK BONE SCREW ANCHOR
Orthopedic
30d
Cleared
Oct 26, 2007
KFX TISSUE FIXATION SYSTEM AND ACCESSORIES
Orthopedic
91d
Cleared
Jul 19, 2006
KFX KNOTLESS FIXATION SYSTEM
Orthopedic
71d