FDA 510(k)

JADE SCORE PTA Scoring Balloon Dilatation Catheter

Número K: K261778 · 2026-09-16

RequerenteOrbusNeich Medical (Shenzhen) Co., Ltd.

Data da decisão2026-09-16

Código do produtoPNO

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

JADE SCORE PTA Scoring Balloon Dilatation Catheter is the device name listed in this FDA 510(k) record. The listed applicant is OrbusNeich Medical (Shenzhen) Co., Ltd.. It received FDA 510(k) clearance on 2026-09-16 under 510(k) number K261778. The device is classified under product code PNO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the JADE SCORE PTA Scoring Balloon Dilatation Catheter?

JADE SCORE PTA Scoring Balloon Dilatation Catheter is a medical device that received FDA 510(k) clearance on 2026-09-16. The listed applicant is OrbusNeich Medical (Shenzhen) Co., Ltd.. The 510(k) number is K261778.

When did JADE SCORE PTA Scoring Balloon Dilatation Catheter receive FDA 510(k) clearance?

JADE SCORE PTA Scoring Balloon Dilatation Catheter received FDA 510(k) clearance on 2026-09-16, under 510(k) number K261778.

Who is the listed applicant for JADE SCORE PTA Scoring Balloon Dilatation Catheter?

The FDA 510(k) record lists OrbusNeich Medical (Shenzhen) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JADE SCORE PTA Scoring Balloon Dilatation Catheter?

O código de produto da FDA para o Balão de Dilatação de Cateter de Scoring PTA JADE SCORE é PNO.

Ensaios clínicos relacionados

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

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

Outros registros que listam OrbusNeich Medical (Shenzhen) Co., Ltd. como candidato(a)

K253361Teleport Glide Microcatheter K242588COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL)K233499Sapphire NC ULTRA Coronary Dilatation Catheter K233505Sapphire ULTRA Coronary Dilatation Catheter K241025JADE PLUS PTA Balloon Dilatation Catheter K231608Teleport XT Microcatheter

Ver todos os 10 dispositivos →

Dispositivos Relacionados (Código: PNO)

K260012UltraScore™ Focused Force PTA BalloonBard Peripheral Vascular, Inc.K243944Cateter de Dilatação Balão PTA NSE ApertaGoodman Co., Ltd.K242254D·Kutting™ LL Peripheral Scoring Balloon Dilatation CatheterDk Medical Technology Co., Ltd.K241478Tri-Wedge PTA Scoring Balloon Dilatation CatheterBrosmed Medical Co., Ltd.K232258XO Constrain™ Percutaneous Transluminal Angioplasty Constraining CatheterTransit Scientific, LLC K232013Catheter de Dilatação Balão PTA NSE Aperta (AW18-05040040/AA18-05040040, AW18-09040040/AA18-09040040, AW18-14540040, AW18-05050040/AA18-05050040, AW18-09050040/AA18-09050040, AW18-14550040, AW18-05060040/AA18-05060040, AW18-09060040/AA18-09060040, AW18-14560040 AW18-05070040/AA18-05070040, AW18-09070040/AA18-09070040, AW18-14570040, AW18-05080040/AA18-05080040, AW18-09080040/AA18-09080040, AW18-14580040)Goodman Co., Ltd.

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.