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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