À propos de cette base de données
Comment utiliser cette base de données
Téléchargez les données
FAQ
Crédits
Devices
Device Recall Stryker Orthopaedics, Duracon XCelerate
Modèle / numéro de série
Catalog number: 8000-7040, all lots
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide Distribution: USA, Sweden, Ireland, Canada, Hong Kong, Germany, Spain, India, Australia, Italy, New Zealand, and United Kingdom.
Description du dispositif
Stryker Orthopaedics, Duracon 4:1 Ceramic Cutting Block LG; || XCelerate cutting block for distal femur in orthopaedic surgery, Non-Sterile.
Manufacturer
Stryker Howmedica Osteonics Corp.
1 Event
Rappel de Device Recall Stryker Orthopaedics, Duracon XCelerate
{{ $t('card.reduce') }}
{{ $tc('card.more', left) }}
Fabricant
Stryker Howmedica Osteonics Corp.
Adresse du fabricant
Stryker Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah NJ 07430
Société-mère du fabricant (2017)
Stryker
Source
USFDA
6 dispositifs médicaux avec un nom similaire
En savoir plus sur les données
ici
Device Recall Stryker Orthopaedics, Duracon XCelerate
Modèle / numéro de série
Catalog Number: 8000-7005, all lots
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide Distribution: USA, Sweden, Ireland, Canada, Hong Kong, Germany, Spain, India, Australia, Italy, New Zealand, and United Kingdom.
Description du dispositif
Stryker Orthopaedics, Duracon 4:1 Ceramic Cutting Block XS; || XCelerate cutting block for distal femur in orthopaedic surgery, Non-Sterile.
Manufacturer
Stryker Howmedica Osteonics Corp.
Device Recall Stryker Orthopaedics, Duracon XCelerate
Modèle / numéro de série
Catalog anumber: 8000-7010, all lots.
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide Distribution: USA, Sweden, Ireland, Canada, Hong Kong, Germany, Spain, India, Australia, Italy, New Zealand, and United Kingdom.
Description du dispositif
Stryker Orthopaedics, Duracon 4:1 Ceramic Cutting Block SM; || XCelerate cutting block for distal femur in orthopaedic surgery, Non-Sterile.
Manufacturer
Stryker Howmedica Osteonics Corp.
Device Recall Stryker Orthopaedics, Duracon XCelerate
Modèle / numéro de série
Catalog number: 8000-7020, all lots.
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide Distribution: USA, Sweden, Ireland, Canada, Hong Kong, Germany, Spain, India, Australia, Italy, New Zealand, and United Kingdom.
Description du dispositif
Stryker Orthopaedics, Duracon 4:1 Ceramic Cutting Block MED; || XCelerate cutting block for distal femur in orthopaedic surgery, Non-Sterile.
Manufacturer
Stryker Howmedica Osteonics Corp.
Device Recall Stryker Orthopaedics, Duracon XCelerate
Modèle / numéro de série
Catalog number: 8000-7030, all lots
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide Distribution: USA, Sweden, Ireland, Canada, Hong Kong, Germany, Spain, India, Australia, Italy, New Zealand, and United Kingdom.
Description du dispositif
Stryker Orthopaedics, Duracon 4:1 Ceramic Cutting Block ML; || XCelerate cutting block for distal femur in orthopaedic surgery, Non-Sterile.
Manufacturer
Stryker Howmedica Osteonics Corp.
Device Recall Stryker Orthopaedics, Duracon XCelerate
Modèle / numéro de série
Catalog number: 8000-7050, all lots
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide Distribution: USA, Sweden, Ireland, Canada, Hong Kong, Germany, Spain, India, Australia, Italy, New Zealand, and United Kingdom.
Description du dispositif
Stryker Orthopaedics, Duracon 4:1 Ceramic Cutting Block XL; || XCelerate cutting block for distal femur in orthopaedic surgery, Non-Sterile.
Manufacturer
Stryker Howmedica Osteonics Corp.
1 de plus
Language
English
Français
Español
한국어