FDA 510(k)

AnyPlus® Spinal Fixation System

N.º K: K172546 · 2017-10-23

Fecha de decisión2017-10-23

Código de productoNKB

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

AnyPlus® Spinal Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is GS Medical Co., Ltd.. It received FDA 510(k) clearance on 2017-10-23 under 510(k) number K172546. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the AnyPlus® Spinal Fixation System?

AnyPlus® Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2017-10-23. The listed applicant is GS Medical Co., Ltd.. The 510(k) number is K172546.

When did AnyPlus® Spinal Fixation System receive FDA 510(k) clearance?

AnyPlus® Spinal Fixation System received FDA 510(k) clearance on 2017-10-23, under 510(k) number K172546.

Who is the listed applicant for AnyPlus® Spinal Fixation System?

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

What is the FDA product code for AnyPlus® Spinal Fixation System?

The FDA product code for AnyPlus® Spinal Fixation System is NKB.

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 GS Medical Co., Ltd. como solicitante

K254260The VEGA Cervical Screw System K243073AnyPlus Sistema de Instrumentos Navegados K241738PYXIS 3D Titanium Cervical Cage system K240350AnyPlus II Sistema de Fijación Espinal K231808QUASAR Standalone ACIF System K223868PYXIS 3D Titanium Cage System

Ver todos los 14 dispositivos →

Dispositivos relacionados (Código: NKB)

K252139Kentrospine Viktr-MIS® Pedicle screw systemRivarp Medical Pvt., Ltd.K262067iFuse Granite Onyx™ Implant SystemSI-BONE, Inc.K262091FRAXION Spinal Fixation SystemOrtler Global Tibbi Gerecler Anonim Sirketi K262193RIVA® Posterior Fixation System with NanoACTIV Surface Technology; RIVA® Anchor Sacroiliac Fixation System with NanoACTIV Surface TechnologyXenix Medical K262828KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.O K260362QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)MANTIZ Co., Ltd.

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.