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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 10 of 15 Results
Applicant: titan spine Decision Date To: 05/10/2019
 
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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® tas interbody fusion device, endoskeleton® tas hyperlordotic interbody fusion device and endoskeleton® tcs interbody fusion device Titan Spine, LLC K173535 02/13/2018
endoskeleton to interbody fusion device (ibd) Titan Spine, LLC K170399 07/06/2017
endoskeleton(r) tas interbody fusion device / endoskeleton(r) tas hyperlordotic interbody fusion device TITAN SPINE, LLC K163269 04/13/2017
endoskeleton(r) tcs system TITAN SPINE, LLC K153122 12/14/2015
endoskeleton tcs interbody fusion device TITAN SPINE, LLC K151596 10/09/2015
endoskeleton tcs system TITAN SPINE, LLC K142940 01/28/2015
endoskeleton; ta ibd and vbr, to and tt, tas, tc, tl TITAN SPINE, LLC K141953 10/27/2014
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(r) tl interbody fusion device TITAN SPINE, LLC K140055 07/02/2014
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