Medical Device Manufacturer · US , Hoffman Estates , IL

Life Spine - FDA 510(k) Cleared Devices

36 submissions · 34 cleared · Since 2006
36
Total
34
Cleared
0
Denied

Life Spine has 34 FDA 510(k) cleared orthopedic devices. Based in Hoffman Estates, US.

Historical record: 34 cleared submissions from 2006 to 2018.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

36 devices
1–12 of 36
Plateau Spacer System
K182470 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar · Orthopedic
Nov 2018 77d
The Life Spine Subtalar Implant System
K160169 · HWC Screw, Fixation, Bone · Orthopedic
Jun 2016 148d
Tarsa-Link Wedge Fixation System
K150368 · HRS Plate, Fixation, Bone · Orthopedic
Mar 2015 40d
PRO-LINK WEDGE SYSTEM
K141905 · HRS Plate, Fixation, Bone · Orthopedic
Sep 2014 73d
LONGBOW SPACER SYSTEM
K133717 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar · Orthopedic
Sep 2014 288d
LIFE SPINE PLATEAU SPACER SYSTEM
K131077 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar · Orthopedic
Jul 2013 91d
NAUTILUS SPINAL SYSTEM
K123373 · NKB Thoracolumbosacral Pedicle Screw System · Orthopedic
Mar 2013 125d
SOLSTICE CROSS CONNECTOR
K120998 · KWP Appliance, Fixation, Spinal Interlaminal · Orthopedic
Oct 2012 182d
NAUTILUS SPINAL SYSTEM
K111953 · NKB Thoracolumbosacral Pedicle Screw System · Orthopedic
Aug 2012 393d
PLATEAU SPACER SYSTEM
K121116 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar · Orthopedic
May 2012 26d
AILERON INTERSPINOUS FIXATION SYSTEM
K113157 · MNI Orthosis, Spinal Pedicle Fixation · Orthopedic
Mar 2012 139d
PLATEAU SPACER SYSTEM
K111569 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar · Orthopedic
Jul 2011 30d
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