Medical Device Manufacturer · US , Fremont , CA

Spine View, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2008
9
Total
9
Cleared
0
Denied

Spine View, Inc. has 9 FDA 510(k) cleared medical devices. Based in Fremont, US.

Historical record: 9 cleared submissions from 2008 to 2016. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Spine View, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Spine View, Inc.
9 devices
1-9 of 9
Cleared Aug 01, 2016
SpineView X-Pac Expandable Lumbar Cage System
K160856 · MAX
Orthopedic · 126d
Cleared Feb 24, 2016
SpineView X-Pac Expandable Lumbar Cage System
K152539 · MAX
Orthopedic · 173d
Cleared Dec 27, 2012
FLEXLITE CAMERA
K122134 · HRX
Orthopedic · 162d
Cleared Aug 16, 2012
SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS)
K121548 · HRX
Orthopedic · 83d
Cleared Jun 26, 2012
ENSPIRE DISCECTOMY SYSTEM
K120680 · HRX
Orthopedic · 112d
Cleared Feb 10, 2012
SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS)
K113362 · HRX
Orthopedic · 87d
Cleared Oct 21, 2011
ENSPIRE DEBRIDER SYSTEM
K110992 · HRX
Orthopedic · 196d
Cleared Apr 15, 2009
ENSPIRE DEBRIDER SYSTEM
K090278 · HRX
Orthopedic · 70d
Cleared Aug 07, 2008
SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS), SPINEVU MINISCOPE
K081051 · HRX
Orthopedic · 115d
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