FDA 510(k)

Ennovate Cervical Spinal and Occiput System

N.º K: K213871 · 2022-07-01

SolicitanteAesculap Implant Systems, LLC

Fecha de decisión2022-07-01

Código de productoNKG

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

Ennovate Cervical Spinal and Occiput System is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap Implant Systems, LLC. It received FDA 510(k) clearance on 2022-07-01 under 510(k) number K213871. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Ennovate Cervical Spinal and Occiput System?

Ennovate Cervical Spinal and Occiput System is a medical device that received FDA 510(k) clearance on 2022-07-01. The listed applicant is Aesculap Implant Systems, LLC. The 510(k) number is K213871.

When did Ennovate Cervical Spinal and Occiput System receive FDA 510(k) clearance?

Ennovate Cervical Spinal and Occiput System received FDA 510(k) clearance on 2022-07-01, under 510(k) number K213871.

Who is the listed applicant for Ennovate Cervical Spinal and Occiput System?

The FDA 510(k) record lists Aesculap Implant Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ennovate Cervical Spinal and Occiput System?

The FDA product code for Ennovate Cervical Spinal and Occiput System is NKG.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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

Otros registros que enlistan a Aesculap Implant Systems, LLC como solicitante

K210963ENNOVATE Spinal System K180433ENNOVATE®K162134ENNOVATE Spinal System K153700Sistemas de Implantes Aesculap(R) (AIS) S4 Instrumentos de Navegación K153396Aesculap OrthoPilot Generación Siguiente

Dispositivos relacionados (Código: NKG)

K254260The VEGA Cervical Screw SystemGS Medical Co., Ltd.K253195TAURUS Posterior Occipital-Cervico-Thoracic Spinal SystemsZheJiang Decans Medical Devices Co., Ltd.K254045CarboClear® Posterior Cervical Screw System; CarboClear® Hybrid Posterior Cervical Screw SystemCarboFix Orthopedics , Ltd.K254165Infinity™ OCT SystemMedtronic Sofamor Danek USA, Inc.K252327CMORE® CT System; CMORE® CT System Navigated InstrumentsIcotec AG K253129Infinity™ OCT SystemMedtronic Sofamor Danek USA, Inc.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.