FDA 510(k)

Articulador Arthroscopic Bur

N.º K: K252666 · 2025-11-21

SolicitanteJoint Preservation Innovations, LLC

Fecha de decisión2025-11-21

Código de productoHRX

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

Articulator Arthroscopic Bur is the device name listed in this FDA 510(k) record. The listed applicant is Joint Preservation Innovations, LLC. It received FDA 510(k) clearance on 2025-11-21 under 510(k) number K252666. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Articulator Arthroscopic Bur?

Articulator Arthroscopic Bur is a medical device that received FDA 510(k) clearance on 2025-11-21. The listed applicant is Joint Preservation Innovations, LLC. The 510(k) number is K252666.

When did Articulator Arthroscopic Bur receive FDA 510(k) clearance?

Articulator Arthroscopic Bur received FDA 510(k) clearance on 2025-11-21, under 510(k) number K252666.

Who is the listed applicant for Articulator Arthroscopic Bur?

The FDA 510(k) record lists Joint Preservation Innovations, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Articulator Arthroscopic Bur?

The FDA product code for Articulator Arthroscopic Bur is HRX.

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

Dispositivos relacionados (Código: HRX)

K260203Fule Vertebroplasty Balloon CatheterBeijing Fule Science & Technology Development Co., Ltd.K254103HOPKINS Telescopes for ArthroscopyKarl Storz SE & CO. KG K252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLC K253523Freedom DS™ Decompression SystemSpinal Simplicity K252546VantageTM Lumbar Decompression KitAllevion Medical, LLC K253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)Medimaging Integrated Solution, Inc (Miis)

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.