Medical Device Manufacturer · US , Good Hope , GA

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

12 submissions · 12 cleared · Since 2001
12
Total
12
Cleared
0
Denied

Spine Vision, Inc. has 12 FDA 510(k) cleared orthopedic devices. Based in Good Hope, US.

Historical record: 12 cleared submissions from 2001 to 2005.

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 - Spine Vision, Inc.
12 devices
1-12 of 12
Cleared Nov 07, 2005
UNI-THREAD SPINAL SYSTEM
K052406 · MNI
Orthopedic · 67d
Cleared Dec 29, 2004
PEDIGUARD NERVE DETECTOR SYSTEM
K030526 · GWF
Neurology · 679d
Cleared Dec 28, 2004
SPACEVISION CAGE SYSTEM
K042930 · MQP
Orthopedic · 67d
Cleared Nov 23, 2004
UNI-THREAD SPINAL SYSTEM
K042640 · MNH
Orthopedic · 57d
Cleared Jan 27, 2004
PLUS PIVOT LINK UNIVERSAL SYSTEM
K033508 · MNI
Orthopedic · 82d
Cleared Oct 31, 2003
PLUS PIVOT LINK UNIVERSAL SYSTEM
K032398 · MNI
Orthopedic · 88d
Cleared Sep 23, 2002
PLUS PIVOT LINK UNIVERSAL SYSTEM
K022271 · MNI
Orthopedic · 72d
Cleared Aug 01, 2002
PLUS PIVOT LINK UNIVERSAL SYSTEM
K021507 · KWP
Orthopedic · 84d
Cleared Aug 01, 2002
UNI-T UNI-THREAD SPINAL SYSTEM
K021510 · MNI
Orthopedic · 84d
Cleared Feb 13, 2002
UNI-T SPINAL SYSTEM
K013301 · MNI
Orthopedic · 133d
Cleared Feb 13, 2002
P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM)
K013312 · KWP
Orthopedic · 132d
Cleared Nov 26, 2001
C3 ANTERIOR CERVICAL PLATE SYSTEM
K012881 · KWQ
Orthopedic · 90d
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