FDA 510(k)

Frontier Medical Devices In-Line Orthopedic Cable Cerclage System

K-Nummer: K153242 · 2016-01-13

AntragstellerFrontier Medical Devices, Inc.

Entscheidungsdatum2016-01-13

ProduktcodeJDQ

BeratungsausschussOR

EntscheidungSubstantially Equivalent

Produktübersicht

Frontier Medical Devices In-Line Orthopedic Cable Cerclage System is the device name listed in this FDA 510(k) record. The listed applicant is Frontier Medical Devices, Inc.. It received FDA 510(k) clearance on 2016-01-13 under 510(k) number K153242. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the Frontier Medical Devices In-Line Orthopedic Cable Cerclage System?

Frontier Medical Devices In-Line Orthopedic Cable Cerclage System is a medical device that received FDA 510(k) clearance on 2016-01-13. The listed applicant is Frontier Medical Devices, Inc.. The 510(k) number is K153242.

When did Frontier Medical Devices In-Line Orthopedic Cable Cerclage System receive FDA 510(k) clearance?

Frontier Medical Devices In-Line Orthopedic Cable Cerclage System received FDA 510(k) clearance on 2016-01-13, under 510(k) number K153242.

Who is the listed applicant for Frontier Medical Devices In-Line Orthopedic Cable Cerclage System?

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

What is the FDA product code for Frontier Medical Devices In-Line Orthopedic Cable Cerclage System?

The FDA product code for Frontier Medical Devices In-Line Orthopedic Cable Cerclage System is JDQ.

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: JDQ)

K261271Cable-Ready® Cable Grip SystemPioneer Surgical Technology, Inc.K243905Stitch Cerclage – Suture TapesGM Dos Reis Industria e Comercio Ltda.K243344Arthrex FiberTape and TigerTape Cerclage Sutures; Arthrex Radiopaque FiberTape Cerclage SuturesArthrex, Inc.K232733Mbrace CableMedacta International S.A.K233949ACCORD Kabel-SystemSmith & Nephew, Inc.K232986VariTrax Sternal CircumFixation SystemCircumfix Solutions, 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.