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FDA 510(k)

Sistema de Navegación de Cirugía de Espina Anatase, Número de modelo: SNS-Spine2-S y SNS-spine2-V

N.º K: K220348 · 2022-07-14

SolicitanteRemex Medical Corporation
Fecha de decisión2022-07-14
Código de productoOLO
Comité asesorNE
DecisiónSubstantially Equivalent

Resumen del dispositivo

Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V is the device name listed in this FDA 510(k) record. The listed applicant is Remex Medical Corporation. It received FDA 510(k) clearance on 2022-07-14 under 510(k) number K220348. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V?

Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V is a medical device that received FDA 510(k) clearance on 2022-07-14. The listed applicant is Remex Medical Corporation. The 510(k) number is K220348.

When did Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V receive FDA 510(k) clearance?

Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V received FDA 510(k) clearance on 2022-07-14, under 510(k) number K220348.

Who is the listed applicant for Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V?

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

What is the FDA product code for Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V?

The FDA product code for Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V is OLO.

Ensayos clínicos relacionados

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Dispositivos relacionados (Código: OLO)

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.

K262506Remex Spine Surgery Navigation - Universal InstrumentsRemex Medical Corp.K261410Navbit MARQ (PRD-001-SUP (Supine Registration Kit), PRD-001-LAT (Lateral Registration Kit))Suite 201, National Innovation CentreK261205SPINEART Navigation Instrument SystemSpineart SAK261024TMINI Miniature Robotic SystemTHINK Surgical, Inc.K262121Ion-L Navigated InstrumentsSurGenTec, LLCK261113Op.n™ Spine Navigation and Robotic GuidanceEcential Robotics

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.

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