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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 10 of 19 Results
Applicant: titan spine Decision Date To: 05/10/2019
 
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endoskeleton ta interbody fusion device, endoskeleton tas and tas hyperlordotic interbody fusion device, endoskeleton to interbody fusion device, endoskeleton tt interbody fusion device, endoskeleton tc interbody fusion device, endoskeleton tcs interbody fusion device, endoskeleton tl interbody fus Titan Spine, Inc K192018 08/16/2019
endoskeleton tas plate Titan Spine, Inc K192054 08/29/2019
endoskeleton tcs interbody fusion device Titan Spine, Inc K191565 08/06/2019
endoskeleton tl interbody fusion device, endoskeleton tl hyperlordotic interbody fusion device Titan Spine, Inc K191581 01/08/2020
endoskeleton® ta interbody fusion device, endoskeleton® tas interbody fusion device, endoskeleton® to interbody fusion device, endoskeleton® tt interbody fusion device, endoskeleton® tc interbody fusion device, endoskeleton® tcs interbody fusion device, endoskeleton® tl interbody fusion device, end Titan Spine, Inc K183557 02/11/2019
endoskeleton ta ibd and vbr, endoskeleton to and tt, endoskeleton tas, endoskeleton tas, endoskeleton tc, endoskeleton tl TITAN SPINE, LLC K142589 10/17/2014
endoskeleton ta interbody fusion device (ibd) TITAN SPINE, LLC K080615 06/17/2008
endoskeleton tc TITAN SPINE, LLC K100889 07/29/2010
endoskeleton tcs interbody fusion device TITAN SPINE, LLC K151596 10/09/2015
endoskeleton tcs system TITAN SPINE, LLC K142940 01/28/2015
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