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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