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FDA 510(k)

Reprocessed ArthoCare Ablation Wand

K-Number: K173741 · 2018-03-05

ApplicantRenovo, Inc.
Decision Date2018-03-05
Product CodeNUJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Reprocessed ArthoCare Ablation Wand is the device name listed in this FDA 510(k) record. The listed applicant is Renovo, Inc.. It received FDA 510(k) clearance on 2018-03-05 under 510(k) number K173741. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reprocessed ArthoCare Ablation Wand?

Reprocessed ArthoCare Ablation Wand is a medical device that received FDA 510(k) clearance on 2018-03-05. The listed applicant is Renovo, Inc.. The 510(k) number is K173741.

When did Reprocessed ArthoCare Ablation Wand receive FDA 510(k) clearance?

Reprocessed ArthoCare Ablation Wand received FDA 510(k) clearance on 2018-03-05, under 510(k) number K173741.

Who is the listed applicant for Reprocessed ArthoCare Ablation Wand?

The FDA 510(k) record lists Renovo, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Reprocessed ArthoCare Ablation Wand?

The FDA product code for Reprocessed ArthoCare Ablation Wand is NUJ.

Other records listing Renovo, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K173740Reprocessed DePuy Mitek Ablation WandK172647Reprocessed ArthroCare ENT CoblatorK172097Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar SleevesK172093Reprocessed Covidien TrocarK172092Reprocessed Shavers/Burs

Related Devices (Code: NUJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K232511Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)Surgical Instrument Service and Savings, Inc.K230251Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability SolutionsK220411Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability SolutionsK211203Green OR Reprocessed Aquamantys Bipolar SealerGreen Or, LLCK191073Vein360 Endovenous Radiofrequency Ablation (RFA) CatheterVein 360, LLCK182588Medline ReNewal Reprocessed LigaSure Maryland Jaw Sealer/DividerSurgical Instrument Service and Savings Inc.(Dba Medline Ren

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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