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Crédits
Devices
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.
1 Event
Rappel de Device Recall Stryker Orthopaedics, Duracon XCelerate
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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
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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 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: 8000-7040, 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.
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.
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