FDA 510(k)

PRADO™ Lumbar Interbody Fusion System

Número K: K252113 · 2025-08-05

Data da decisão2025-08-05

Código do produtoMAX

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

PRADO™ Lumbar Interbody Fusion System is the device name listed in this FDA 510(k) record. The listed applicant is Bethesda Medical Devices. It received FDA 510(k) clearance on 2025-08-05 under 510(k) number K252113. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the PRADO™ Lumbar Interbody Fusion System?

PRADO™ Lumbar Interbody Fusion System is a medical device that received FDA 510(k) clearance on 2025-08-05. The listed applicant is Bethesda Medical Devices. The 510(k) number is K252113.

When did PRADO™ Lumbar Interbody Fusion System receive FDA 510(k) clearance?

PRADO™ Lumbar Interbody Fusion System received FDA 510(k) clearance on 2025-08-05, under 510(k) number K252113.

Who is the listed applicant for PRADO™ Lumbar Interbody Fusion System?

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

What is the FDA product code for PRADO™ Lumbar Interbody Fusion System?

The FDA product code for PRADO™ Lumbar Interbody Fusion System is MAX.

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: MAX)

K261049SCALA® TLSpineart SA K261430TruLift Expandable SystemLife Spine, Inc.K253011Catalyft PL Expandable Interbody SystemMedtronic Sofamor Danek USA, Inc.K261020Symmetrix™ L Spinal SystemMedtronic Sofamor Danek USA, Inc.K253420Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody SystemSeaSpine Orthopedics Corporation K253151Fule Interbody Fusion Cage SystemBeijing Fule Science & Technology Development 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.