FDA 510(k)

Reef L Interbody System; WaveForm L Interbody System

N.º K: K240566 · 2024-04-26

SolicitanteSeaSpine Orthopedics Corporation

Fecha de decisión2024-04-26

Código de productoMAX

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

Reef L Interbody System; WaveForm L Interbody System is the device name listed in this FDA 510(k) record. The listed applicant is SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2024-04-26 under 510(k) number K240566. 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 Reef L Interbody System; WaveForm L Interbody System?

Reef L Interbody System; WaveForm L Interbody System is a medical device that received FDA 510(k) clearance on 2024-04-26. The listed applicant is SeaSpine Orthopedics Corporation. The 510(k) number is K240566.

When did Reef L Interbody System; WaveForm L Interbody System receive FDA 510(k) clearance?

Reef L Interbody System; WaveForm L Interbody System received FDA 510(k) clearance on 2024-04-26, under 510(k) number K240566.

Who is the listed applicant for Reef L Interbody System; WaveForm L Interbody System?

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

What is the FDA product code for Reef L Interbody System; WaveForm L Interbody System?

The FDA product code for Reef L Interbody System; WaveForm L Interbody System is MAX.

Ensayos clínicos relacionados

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Otros registros que enlistan a SeaSpine Orthopedics Corporation como solicitante

K253420Sistema Admiral ACP; Sistema Explorer TO; Sistema de Laminoplastia; Espaciador TDF Manta Ray; Sistema Interbody Meridian; Sistema de Placa Anterior Meridian; Sistema Interbody L Reef; Sistema TO/TA Reef; Sistema Lateral Regatta; Sistema de Placa Lateral Regatta; Sistema Interbody ACS Shoreline; Placa TruProfile Entornada Shoreline; Sistema Interbody RT Shoreline; Malla Vu; Sistema Interbody A WaveForm; Sistema Interbody C WaveForm; Sistema Interbody L WaveForm; Sistema Interbody TA WaveForm; Sistema Interbody TO WaveForm K250908Virata Spinal Fixation System K243659FLASH™ Facet Fusion Instruments, IsoTis® Facet Fusion Instruments K242273Cove Putty, OsteoCove Putty K241466Shoreline ACS Interbody System; Shoreline RT Interbody System; Regatta Lateral System; Reef L Interbody System; Reef TO/TA System; Meridian Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TO Interbody System; WaveForm TA Interbody System; WaveForm A Interbody System K232566NewPort Spinal System; Daytona Small Stature Spinal System; Malibu Spinal System; Mariner Pedicle Screw Systems: Mariner Outrigger Revision System; Mariner MIS Pedicle Screw System; Mariner Deformity System; Mariner RDX System

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Dispositivos relacionados (Código: MAX)

Fuente oficial

Ver en la base de datos de la FDA →

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