Reprocessed ArthoCare Ablation Wand— 510(k) K173741

Substantially Equivalent

Renovo, Inc.

FDA 510(k) clearance K173741 for Reprocessed ArthoCare Ablation Wand, Substantially Equivalent on 2018-03-05. Applicant: Renovo, Inc..

Clearance details

Applicant: Renovo, Inc.
Product code: Code NUJ
Advisory panel: General, Plastic Surgery
Date received: 2017-12-07
Decision date: 2018-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bend, OR, US

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