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FDA 510(k) Applications Submitted by ReNovo, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K172092
07/11/2017
Reprocessed Shavers/Burs
Renovo, Inc.
K172093
07/11/2017
Reprocessed Covidien Trocar
Renovo, Inc.
K172097
07/11/2017
Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves
Renovo, Inc.
K172647
09/01/2017
Reprocessed ArthroCare ENT Coblator
ReNovo, Inc.
K173740
12/07/2017
Reprocessed DePuy Mitek Ablation Wand
ReNovo, Inc.
K173741
12/07/2017
Reprocessed ArthoCare Ablation Wand
ReNovo, Inc.
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