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FDA 510(k)

CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)

N.º K: K152509 · 2016-01-12

SolicitanteAltatec GmbH
Fecha de decisión2016-01-12
Código de productoNHA
Comité asesorDE
DecisiónSubstantially Equivalent

Resumen del dispositivo

CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) is the device name listed in this FDA 510(k) record. The listed applicant is Altatec GmbH. It received FDA 510(k) clearance on 2016-01-12 under 510(k) number K152509. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)?

CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) is a medical device that received FDA 510(k) clearance on 2016-01-12. The listed applicant is Altatec GmbH. The 510(k) number is K152509.

When did CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) receive FDA 510(k) clearance?

CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) received FDA 510(k) clearance on 2016-01-12, under 510(k) number K152509.

Who is the listed applicant for CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)?

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

What is the FDA product code for CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)?

The FDA product code for CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) is NHA.

Ensayos clínicos relacionados

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Otros registros que enlistan a Altatec GmbH 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.

K193401Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE ImplantesK160784CAM Titanium BlanksK153779Soporte para Puentes

Dispositivos relacionados (Código: NHA)

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.

K262207Cemented Plus AbutmentUnidental Co., Ltd.K260940BellaTek BarsZimVie US Corp, LLCK253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare ABK261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, Inc.

Fuente oficial

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Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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