Life Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Life Spine - FDA 510(k) Cleared Devices
Recent clearances: Plateau Spacer System
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) Regulatory Record - Life Spine
36 devices
Cleared
Nov 26, 2018
Plateau Spacer System
Orthopedic
77d
Cleared
Jun 23, 2016
The Life Spine Subtalar Implant System
Orthopedic
148d
Cleared
Mar 24, 2015
Tarsa-Link Wedge Fixation System
Orthopedic
40d
Cleared
Sep 26, 2014
PRO-LINK WEDGE SYSTEM
Orthopedic
73d
Cleared
Sep 19, 2014
LONGBOW SPACER SYSTEM
Orthopedic
288d
Cleared
Jul 17, 2013
LIFE SPINE PLATEAU SPACER SYSTEM
Orthopedic
91d
Cleared
Mar 06, 2013
NAUTILUS SPINAL SYSTEM
Orthopedic
125d
Cleared
Oct 01, 2012
SOLSTICE CROSS CONNECTOR
Orthopedic
182d
Cleared
Aug 07, 2012
NAUTILUS SPINAL SYSTEM
Orthopedic
393d
Cleared
May 08, 2012
PLATEAU SPACER SYSTEM
Orthopedic
26d
Cleared
Mar 13, 2012
AILERON INTERSPINOUS FIXATION SYSTEM
Orthopedic
139d
Cleared
Jul 06, 2011
PLATEAU SPACER SYSTEM
Orthopedic
30d