FDA 510(k)

Mochida Nerve Cuff

Número K: K233322 · 2024-06-21

RequerenteMochida Pharmaceutical Co., Ltd.

Data da decisão2024-06-21

Código do produtoJXI

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Mochida Nerve Cuff is the device name listed in this FDA 510(k) record. The listed applicant is Mochida Pharmaceutical Co., Ltd.. It received FDA 510(k) clearance on 2024-06-21 under 510(k) number K233322. The device is classified under product code JXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Mochida Nerve Cuff?

Mochida Nerve Cuff is a medical device that received FDA 510(k) clearance on 2024-06-21. The listed applicant is Mochida Pharmaceutical Co., Ltd.. The 510(k) number is K233322.

When did Mochida Nerve Cuff receive FDA 510(k) clearance?

Mochida Nerve Cuff received FDA 510(k) clearance on 2024-06-21, under 510(k) number K233322.

Who is the listed applicant for Mochida Nerve Cuff?

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

What is the FDA product code for Mochida Nerve Cuff?

The FDA product code for Mochida Nerve Cuff is JXI.

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: JXI)

K260245SILKBridgeKLISBio S.r.l.K253363NeuroSpan BridgeAuxilium Biotechnologies, Inc.K251505VersaCoat Nerve Protector (VTP-44G2); VersaCoat Nerve Protector (VTP-12G1)Alafair Biosciences K251175VersaWrap Nerve Protector (VTP-2201); VersaWrap Nerve Protector (VTP-1201)Alafair Biosciences K242113Nerve Wrap (07-DW-001-TAB)Biocircuit Technologies, Inc.K243889Remplir (ON-152, 15 x 20 mm); Remplir (ON-203, 20 x 30 mm); Remplir (ON-304, 30 x 40 mm); Remplir (ON-405, 40 x 50 mm)Orthocell, 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.