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FDA 510(k) Applications Submitted by NLT SPINE LTD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K151654
06/18/2015
PROW FUSION
NLT SPINE LTD
K153665
12/21/2015
PROW FUSION-L
NLT SPINE LTD
K153786
12/31/2015
PROW FUSION-V
NLT SPINE LTD
K130057
01/09/2013
ESPIN
NLT SPINE LTD
K120553
02/23/2012
ESPIN
NLT SPINE LTD
K112359
08/16/2011
PROW FUSION
NLT SPINE LTD
K133061
09/27/2013
ESPIN SYSTEM
NLT SPINE LTD
K130254
02/01/2013
PROW FUSION
NLT SPINE LTD
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