Spine Smith Partners L.P. is one of 16247 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spine Smith Partners L.P. - FDA 510(k) Cleared Devices
Recent clearances: IN:C2 SPINAL FIXATION SYSTEM, VISUALIF CHALLENGING ACCESS PLATE, SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEM
9
Total
9
Cleared
0
Denied
Spine Smith Partners L.P. has 9 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 9 cleared submissions from 2008 to 2012. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spine Smith Partners L.P. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spine Smith Partners L.P.
9 devices
Cleared
Dec 05, 2012
IN:C2 SPINAL FIXATION SYSTEM
Orthopedic
99d
Cleared
Oct 11, 2012
VISUALIF CHALLENGING ACCESS PLATE
Orthopedic
80d
Cleared
Sep 30, 2010
SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEM
Orthopedic
66d
Cleared
Jul 01, 2010
SPINESMITH CYNCH SPINAL SYSTEM
Orthopedic
73d
Cleared
Apr 01, 2009
SPINESMITH CYNCH SPINAL SYSTEM
Orthopedic
43d
Cleared
Oct 31, 2008
SPINESMITH PARTNERS, LP CEQUENCE ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
36d
Cleared
Jul 14, 2008
SPINESMITH PARTNERS, LP CEQUENCE ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
84d
Cleared
Jul 02, 2008
SPINESMITH CIMPLICITY SPINAL SYSTEM
Orthopedic
89d
Cleared
Feb 07, 2008
CIMPLICITY SPINAL SYSTEM
Orthopedic
73d