I.B.S. osteosynthesis screws — 510(k) de la FDA K170594

Resumen del dispositivo

I.B.S. osteosynthesis screws is the device name listed in this FDA 510(k) record. The listed applicant is In2bones Sas. It received FDA 510(k) clearance on 2017-05-10 under 510(k) number K170594. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the I.B.S. osteosynthesis screws?

I.B.S. osteosynthesis screws is a medical device that received FDA 510(k) clearance on 2017-05-10. The listed applicant is In2bones Sas. The 510(k) number is K170594.

When did I.B.S. osteosynthesis screws receive FDA 510(k) clearance?

I.B.S. osteosynthesis screws received FDA 510(k) clearance on 2017-05-10, under 510(k) number K170594.

Who is the listed applicant for I.B.S. osteosynthesis screws?

The FDA 510(k) record lists In2bones Sas as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I.B.S. osteosynthesis screws?

The FDA product code for I.B.S. osteosynthesis screws is HWC. This falls under the Cardiovascular category.

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 In2bones Sas como solicitante

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.

K231699QUANTUM® Patient Specific Instrumentation (PSI) System K230313QUANTUM Patient Specific Instrumentation (PSI) System K211883QUANTUM® Patient Specific Instrumentation (PSI) System K191380Quantum® Total Ankle Prosthesis K173811TRIWAY Tibiotalocalcaneal (TTC) Arthrodesis System K173616DIP Arthrodesis System

Ver todos los 14 dispositivos →

Dispositivos relacionados (Código: HWC)

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.

K262975Sistema Arthrex BeamingArthrex, Inc.K260995DynaNail Helix® Fixation SystemMedShape, Inc.K254280F.A.S.T ScrewSteps Ortho K261057ActivaScrew™ Cannulated COMBioretec, Ltd.K260106OsteoCoil™ GT Active Compression SystemFlower Orthopedics Corporation DBA Conventus Flower Orthoped K262344Large Compression ScrewsTriMed, Inc.

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.