Vertebron, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vertebron, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Vertebron, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in Stratford, US.
Historical record: 11 cleared submissions from 2004 to 2008.
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 - Vertebron, Inc.
11 devices
Cleared
Jul 03, 2008
VERTEBRON SSP CERVICAL PLATING SYSTEM
Orthopedic
29d
Cleared
Jul 02, 2008
MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM
Orthopedic
26d
Cleared
Mar 24, 2008
VERTEBRON VBR SYSTEM
Orthopedic
102d
Cleared
Jun 13, 2007
MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM
Orthopedic
27d
Cleared
Aug 16, 2006
VERTEBRON SCP CERVICAL PLATE SYSTEM
Orthopedic
23d
Cleared
Oct 17, 2005
MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM
Orthopedic
104d
Cleared
Sep 07, 2005
VERTEBRON PSS PEDICLE SCREW SYSTEM
Orthopedic
72d
Cleared
Feb 01, 2005
VERTEBRON PSS PEDICLE SCREW SYSTEM
Orthopedic
78d
Cleared
Dec 17, 2004
MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM
Orthopedic
30d
Cleared
Mar 26, 2004
VERTEBRON SCP CERVICAL PLATE SYSTEM
Orthopedic
84d
Cleared
Feb 25, 2004
VERTEBRON PSS PEDICLE SCREW SYSTEM
Orthopedic
128d