FDA 510(k)

MedCAD® AccuPlate® Patient-Specific Plate

Número K: K193280 · 2021-02-12

RequerenteMedcad

Data da decisão2021-02-12

Código do produtoJEY

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

MedCAD® AccuPlate® Patient-Specific Plate is the device name listed in this FDA 510(k) record. The listed applicant is Medcad. It received FDA 510(k) clearance on 2021-02-12 under 510(k) number K193280. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the MedCAD® AccuPlate® Patient-Specific Plate?

MedCAD® AccuPlate® Patient-Specific Plate is a medical device that received FDA 510(k) clearance on 2021-02-12. The listed applicant is Medcad. The 510(k) number is K193280.

When did MedCAD® AccuPlate® Patient-Specific Plate receive FDA 510(k) clearance?

MedCAD® AccuPlate® Patient-Specific Plate received FDA 510(k) clearance on 2021-02-12, under 510(k) number K193280.

Who is the listed applicant for MedCAD® AccuPlate® Patient-Specific Plate?

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

What is the FDA product code for MedCAD® AccuPlate® Patient-Specific Plate?

The FDA product code for MedCAD® AccuPlate® Patient-Specific Plate is JEY.

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 Medcad como candidato(a)

K252064MedCAD® AccuStride™ System K251709MedCAD® AccuStride™ System K241811MedCAD® AccuStride™ System K230398MedCAD® AccuPlate® 3DTi Patient-Specific Plating System K223421MedCAD AccuPlan Orthopedics System K223024MedCAD AccuPlan System

Ver todos os 9 dispositivos →

Dispositivos Relacionados (Código: JEY)

K260137KLS Martin IPS Oral-Max Implants - MR Conditional; Individual Patient Solutions - Ti (IPS-Ti); Individual Patient Solutions - PEEK (IPS-PEEK); KLS Martin Individual Patient SolutionsKLS-Martin L.P.K253206METICULY Patient-specific CMF solutionMeticuly Co., Ltd.K252246Leforte MMF SystemJeil Medical Corporation K253373Southern Craniomaxillofacial (CMF) SystemSouthern Medical (Pty) , Ltd.K251441Inion CPS 1.5 Baby Bioabsorbable Fixation System; Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation SystemInion OY K241314KLS Martin Oral-Max Implants MR Conditional (bundled)KLS-Martin L.P.

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.