FDA 510(k)

Precision Casting Solutions Total Knee System

Número K: K190355 · 2019-05-16

RequerentePrecision Casting Solutions, Inc.

Data da decisão2019-05-16

Código do produtoJWH

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Precision Casting Solutions Total Knee System is the device name listed in this FDA 510(k) record. The listed applicant is Precision Casting Solutions, Inc.. It received FDA 510(k) clearance on 2019-05-16 under 510(k) number K190355. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Precision Casting Solutions Total Knee System?

Precision Casting Solutions Total Knee System is a medical device that received FDA 510(k) clearance on 2019-05-16. The listed applicant is Precision Casting Solutions, Inc.. The 510(k) number is K190355.

When did Precision Casting Solutions Total Knee System receive FDA 510(k) clearance?

Precision Casting Solutions Total Knee System received FDA 510(k) clearance on 2019-05-16, under 510(k) number K190355.

Who is the listed applicant for Precision Casting Solutions Total Knee System?

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

What is the FDA product code for Precision Casting Solutions Total Knee System?

The FDA product code for Precision Casting Solutions Total Knee System is JWH.

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

Dispositivos Relacionados (Código: JWH)

K262057GMK ExtensionMedacta International SA K260063GSPE SpacerThe General Hospital Corporation, d/b/a Massachusetts K262293EVOLUTION MPX™ Total Knee SystemSuzhou Microport Orthorecon Co., Ltd.K262341b-ONE® Mobio™ Total Knee System Revision Cemented Tibial Augments, Stem Extensions and Press-Fit Stem ExtensionsB-One Ortho, Corp.K262130ATTUNE Sistema de Quadril de RevisãoDepuy Orthopaedics, Inc.K253961SK Knee SystemJust Medical Devices (Tianjin) 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.