FDA 510(k)

Symmetrix™ L Spinal System

N.º K: K261020 · 2026-07-14

SolicitanteMedtronic Sofamor Danek USA, Inc.

Fecha de decisión2026-07-14

Código de productoMAX

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

Symmetrix™ L Spinal System is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Sofamor Danek USA, Inc.. It received FDA 510(k) clearance on 2026-07-14 under 510(k) number K261020. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Symmetrix™ L Spinal System?

Symmetrix™ L Spinal System is a medical device that received FDA 510(k) clearance on 2026-07-14. The listed applicant is Medtronic Sofamor Danek USA, Inc.. The 510(k) number is K261020.

When did Symmetrix™ L Spinal System receive FDA 510(k) clearance?

Symmetrix™ L Spinal System received FDA 510(k) clearance on 2026-07-14, under 510(k) number K261020.

Who is the listed applicant for Symmetrix™ L Spinal System?

The FDA 510(k) record lists Medtronic Sofamor Danek USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Symmetrix™ L Spinal System?

The FDA product code for Symmetrix™ L Spinal System is MAX.

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Otros registros que enlistan a Medtronic Sofamor Danek USA, Inc. como solicitante

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Dispositivos relacionados (Código: MAX)

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Fuente oficial

Ver en la base de datos de la FDA →

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