Reprocessed ArthroCare ENT Coblator— 510(k) K172647

Substantially Equivalent

Renovo, Inc.

FDA 510(k) clearance K172647 for Reprocessed ArthroCare ENT Coblator, Substantially Equivalent on 2018-02-21. Applicant: Renovo, Inc..

Clearance details

Applicant: Renovo, Inc.
Product code: Code NUJ
Advisory panel: General, Plastic Surgery
Date received: 2017-09-01
Decision date: 2018-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bend, OR, US

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