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.

FDA 510(k) cleared devices by Life Spine

36 devices
1-12 of 36
Cleared Nov 26, 2018
Plateau Spacer System
K182470 · MAX
Orthopedic · 77d
Cleared Jun 23, 2016
The Life Spine Subtalar Implant System
K160169 · HWC
Orthopedic · 148d
Cleared Mar 24, 2015
Tarsa-Link Wedge Fixation System
K150368 · HRS
Orthopedic · 40d
Cleared Sep 26, 2014
PRO-LINK WEDGE SYSTEM
K141905 · HRS
Orthopedic · 73d
Cleared Sep 19, 2014
LONGBOW SPACER SYSTEM
K133717 · MAX
Orthopedic · 288d
Cleared Jul 17, 2013
LIFE SPINE PLATEAU SPACER SYSTEM
K131077 · MAX
Orthopedic · 91d
Cleared Mar 06, 2013
NAUTILUS SPINAL SYSTEM
K123373 · NKB
Orthopedic · 125d
Cleared Oct 01, 2012
SOLSTICE CROSS CONNECTOR
K120998 · KWP
Orthopedic · 182d
Cleared Aug 07, 2012
NAUTILUS SPINAL SYSTEM
K111953 · NKB
Orthopedic · 393d
Cleared May 08, 2012
PLATEAU SPACER SYSTEM
K121116 · MAX
Orthopedic · 26d
Cleared Mar 13, 2012
AILERON INTERSPINOUS FIXATION SYSTEM
K113157 · MNI
Orthopedic · 139d
Cleared Jul 06, 2011
PLATEAU SPACER SYSTEM
K111569 · MAX
Orthopedic · 30d
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