Medical Device Manufacturer · US , Stratford , CT

Vertebron, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2004
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
1-11 of 11
Cleared Jul 03, 2008
VERTEBRON SSP CERVICAL PLATING SYSTEM
K081567 · KWQ
Orthopedic · 29d
Cleared Jul 02, 2008
MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM
K081597 · MNI
Orthopedic · 26d
Cleared Mar 24, 2008
VERTEBRON VBR SYSTEM
K073502 · MQP
Orthopedic · 102d
Cleared Jun 13, 2007
MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM
K071376 · NKB
Orthopedic · 27d
Cleared Aug 16, 2006
VERTEBRON SCP CERVICAL PLATE SYSTEM
K062110 · KWQ
Orthopedic · 23d
Cleared Oct 17, 2005
MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM
K051815 · KWQ
Orthopedic · 104d
Cleared Sep 07, 2005
VERTEBRON PSS PEDICLE SCREW SYSTEM
K051716 · KWP
Orthopedic · 72d
Cleared Feb 01, 2005
VERTEBRON PSS PEDICLE SCREW SYSTEM
K043152 · MNH
Orthopedic · 78d
Cleared Dec 17, 2004
MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM
K043181 · KWQ
Orthopedic · 30d
Cleared Mar 26, 2004
VERTEBRON SCP CERVICAL PLATE SYSTEM
K040003 · KWQ
Orthopedic · 84d
Cleared Feb 25, 2004
VERTEBRON PSS PEDICLE SCREW SYSTEM
K033352 · MNI
Orthopedic · 128d
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