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FDA 510(k) Applications Submitted by AgNovos Healthcare USA, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K181342
05/21/2018
JGH1 Bone Graft Substitute
AgNovos Healthcare USA, LLC
K181585
06/15/2018
JGH1 Core Deccompression Procedure Kit
AgNovos Healthcare USA, LLC
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