Spine Vision, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spine Vision, Inc. - FDA 510(k) Cleared Devices
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
Cleared
Nov 07, 2005
UNI-THREAD SPINAL SYSTEM
Orthopedic
67d
Cleared
Dec 29, 2004
PEDIGUARD NERVE DETECTOR SYSTEM
Neurology
679d
Cleared
Dec 28, 2004
SPACEVISION CAGE SYSTEM
Orthopedic
67d
Cleared
Nov 23, 2004
UNI-THREAD SPINAL SYSTEM
Orthopedic
57d
Cleared
Jan 27, 2004
PLUS PIVOT LINK UNIVERSAL SYSTEM
Orthopedic
82d
Cleared
Oct 31, 2003
PLUS PIVOT LINK UNIVERSAL SYSTEM
Orthopedic
88d
Cleared
Sep 23, 2002
PLUS PIVOT LINK UNIVERSAL SYSTEM
Orthopedic
72d
Cleared
Aug 01, 2002
PLUS PIVOT LINK UNIVERSAL SYSTEM
Orthopedic
84d
Cleared
Aug 01, 2002
UNI-T UNI-THREAD SPINAL SYSTEM
Orthopedic
84d
Cleared
Feb 13, 2002
UNI-T SPINAL SYSTEM
Orthopedic
133d
Cleared
Feb 13, 2002
P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM)
Orthopedic
132d
Cleared
Nov 26, 2001
C3 ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
90d