FDA 510(k)

ExsoMed ArcPhix and ExsoMed ArrowPhix

K-Nummer: K171407 · 2017-08-18

AntragstellerExsomed Holding Company, LLC

Entscheidungsdatum2017-08-18

ProduktcodeHWC

BeratungsausschussOR

EntscheidungSubstantially Equivalent

Produktübersicht

ExsoMed ArcPhix and ExsoMed ArrowPhix is the device name listed in this FDA 510(k) record. The listed applicant is Exsomed Holding Company, LLC. It received FDA 510(k) clearance on 2017-08-18 under 510(k) number K171407. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the ExsoMed ArcPhix and ExsoMed ArrowPhix?

ExsoMed ArcPhix and ExsoMed ArrowPhix is a medical device that received FDA 510(k) clearance on 2017-08-18. The listed applicant is Exsomed Holding Company, LLC. The 510(k) number is K171407.

When did ExsoMed ArcPhix and ExsoMed ArrowPhix receive FDA 510(k) clearance?

ExsoMed ArcPhix and ExsoMed ArrowPhix received FDA 510(k) clearance on 2017-08-18, under 510(k) number K171407.

Who is the listed applicant for ExsoMed ArcPhix and ExsoMed ArrowPhix?

The FDA 510(k) record lists Exsomed Holding Company, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ExsoMed ArcPhix and ExsoMed ArrowPhix?

The FDA product code for ExsoMed ArcPhix and ExsoMed ArrowPhix is HWC. This falls under the Cardiovascular category.

Zugehörige klinische Studien

Zugehörige Einträge werden automatisch anhand von Namen, Produktcodes oder anderen Metadaten abgeglichen. Eine Übereinstimmung begründet kein verifiziertes klinisches, wissenschaftliches, unternehmerisches oder regulatorisches Verhältnis; prüfen Sie die verlinkten offiziellen Quellen.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Verwandte Geräte (Code: HWC)

K262975Arthrex Beaming-SystemArthrex, Inc.K260995DynaNail Helix® Fixation SystemMedShape, Inc.K254280F.A.S.T ScrewSteps Ortho K261057ActivaScrew™ Cannulated COMBioretec, Ltd.K260106OsteoCoil™ GT Active Compression SystemFlower Orthopedics Corporation DBA Conventus Flower Orthoped K262344Large Compression ScrewsTriMed, Inc.

Offizielle Quelle

In der FDA-Datenbank anzeigen →

Daten aus der FDA Open API. Für die aktuellsten und verbindlichen Informationen konsultieren Sie bitte stets den offiziellen Datensatz.