Medical Device Manufacturer · US , Austin , TX

Spine Smith Partners L.P. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2008
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
1-9 of 9
Cleared Dec 05, 2012
IN:C2 SPINAL FIXATION SYSTEM
K122630 · OVE
Orthopedic · 99d
Cleared Oct 11, 2012
VISUALIF CHALLENGING ACCESS PLATE
K122168 · OVD
Orthopedic · 80d
Cleared Sep 30, 2010
SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEM
K102090 · OVD
Orthopedic · 66d
Cleared Jul 01, 2010
SPINESMITH CYNCH SPINAL SYSTEM
K101085 · MAX
Orthopedic · 73d
Cleared Apr 01, 2009
SPINESMITH CYNCH SPINAL SYSTEM
K090376 · MAX
Orthopedic · 43d
Cleared Oct 31, 2008
SPINESMITH PARTNERS, LP CEQUENCE ANTERIOR CERVICAL PLATE SYSTEM
K082821 · KWQ
Orthopedic · 36d
Cleared Jul 14, 2008
SPINESMITH PARTNERS, LP CEQUENCE ANTERIOR CERVICAL PLATE SYSTEM
K081132 · KWQ
Orthopedic · 84d
Cleared Jul 02, 2008
SPINESMITH CIMPLICITY SPINAL SYSTEM
K080971 · MQP
Orthopedic · 89d
Cleared Feb 07, 2008
CIMPLICITY SPINAL SYSTEM
K073320 · ODP
Orthopedic · 73d
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