FDA 510(k)

Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs)

N.º K: K242543 · 2024-11-22

Fecha de decisión2024-11-22

Código de productoMBH

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs) is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2024-11-22 under 510(k) number K242543. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs)?

Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs) is a medical device that received FDA 510(k) clearance on 2024-11-22. The listed applicant is Zimmer, Inc.. The 510(k) number is K242543.

When did Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs) receive FDA 510(k) clearance?

Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs) received FDA 510(k) clearance on 2024-11-22, under 510(k) number K242543.

Who is the listed applicant for Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs)?

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

What is the FDA product code for Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs)?

The FDA product code for Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs) is MBH.

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 Zimmer, Inc. como solicitante

K262955OsseoFit Stemless Shoulder System K261683Augment Off-Axis Instrument System K260831Z1 Hip System K251840Zimmer® Persona® Personalized Knee System K260182Avenir® Müller Stem; Avenir Complete™ Hip System K253592Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)

Ver todos los 61 dispositivos →

Dispositivos relacionados (Código: MBH)

K261275Unity Total Knee System, Unity Knee Cementless CR FemurCorin, Ltd.K261462LANDMARK Total Knee SystemSmith & Nephew, Inc.K253728EVOLUTION® AM BIOFOAM® Tibial SystemMicroport Orthopedics, Inc.K251840Zimmer® Persona® Personalized Knee SystemZimmer, Inc.K253189Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs)Zimmer, Inc.K253328GMK 3D Metal Tibial Tray ExtensionMedacta International S.A.

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.