Medical Device Manufacturer · US , West Chester , PA

Synthes Spine Co.Lp - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 2005
18
Total
18
Cleared
0
Denied

Synthes Spine Co.Lp has 18 FDA 510(k) cleared orthopedic devices. Based in West Chester, US.

Historical record: 18 cleared submissions from 2005 to 2012.

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 - Synthes Spine Co.Lp
18 devices
1-18 of 18
Cleared Jul 25, 2012
SYNTHES ZERO-P VARIABLE ANGLE (VA)
K121852 · OVE
Orthopedic · 30d
Cleared Dec 12, 2011
SYNTHES ZERO-P
K112459 · OVE
Orthopedic · 108d
Cleared Nov 07, 2011
SYNTHES ZERO-P VARIABLE ANGLE (VA)
K112068 · OVE
Orthopedic · 110d
Cleared Oct 20, 2011
SYNTHES XRL
K103320 · MQP
Orthopedic · 342d
Cleared Sep 02, 2008
ANTEGRA-T
K081568 · KWQ
Orthopedic · 90d
Cleared May 23, 2008
ARCOFIX
K080020 · KWQ
Orthopedic · 141d
Cleared Feb 11, 2008
SYNTHES ZERO-P
K072981 · OVE
Orthopedic · 111d
Cleared Jan 10, 2008
SYNTHES OC FUSION AND SYNAPSE SYSTEMS
K072434 · MNI
Orthopedic · 134d
Cleared Oct 12, 2007
SYNFIX-LR SPACER
K072253 · OVD
Orthopedic · 59d
Cleared Jun 08, 2007
SYNAPSE SYSTEM
K070573 · MNI
Orthopedic · 100d
Cleared Apr 03, 2007
SYNFIX -LR
K062083 · MQP
Orthopedic · 256d
Cleared Jan 31, 2007
SYNTHES ORACLE SPACER
K062933 · MQP
Orthopedic · 125d
Cleared Nov 14, 2006
SYNTHES ANTEGRA SYSTEM
K063158 · KWQ
Orthopedic · 28d
Cleared Sep 06, 2006
SYNTHES OC FUSION SYSTEM
K053418 · KWP
Orthopedic · 272d
Cleared Aug 18, 2006
SYNEX II
K061891 · MQP
Orthopedic · 46d
Cleared Feb 13, 2006
SYNFIX-LR
K053508 · MQP
Orthopedic · 59d
Cleared Dec 07, 2005
SYNTHES PANGEA MONOAXIAL SYSTEM
K052151 · NKB
Orthopedic · 121d
Cleared Mar 24, 2005
SYNTHES VECTRA SYSTEM
K050451 · KWQ
Orthopedic · 30d
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