MEDTRONIC SPINE LLC

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Description

4 dispositivos en la base de datos

  • Modelo / Serial
    Model Catalog: K16B (Lot serial: J6031601); Model Catalog: K16A (Lot serial: J6031601); Model Catalog: K16B (Lot serial: J6013008); Model Catalog: K16A (Lot serial: J6013008); Model Catalog: K16B (Lot serial: J5121206); Model Catalog: K16A (Lot serial: J6031008); Model Catalog: K16B (Lot serial: J6031008); Model Catalog: K16A (Lot serial: J5121206); Model Catalog: KPT0003 (Lot serial: J5120910); Model Catalog: K17B (Lot serial: J6010906); Model Catalog: K17B (Lot serial: J6041202); Model Catalog: K17A (Lot serial: J6041202); Model Catalog: K17B (Lot serial: J6032201); Model Catalog: K17A (Lot serial: J6032201); Model Catalog: K17B (Lot serial: J6030128); Model Catalog: K17A (Lot serial: J6030128); Model Catalog: K17B (Lot serial: J6021511); Model Catalog: K17A (Lot serial: J6021511); Model Catalog: KPT0001 (Lot serial: J5121504); Model Catalog: K17A (Lot serial: J6010906); Model Catalog: K17B (Lot serial: J6031009); Model Catalog: K17A (Lot serial: J6031009); Model Catalog: K17B (Lot serial: J6021706); Model
  • Descripción del producto
    KyphX Elevate Inflatable Bone Tamp
  • Modelo / Serial
    Model Catalog: C01B (Lot serial: J7102403)
  • Descripción del producto
    KYPHX HV-R BONE CEMENT W/ KYPHON MIXER
  • Modelo / Serial
    Model Catalog: C01A (Lot serial: EL08304)
  • Descripción del producto
    KyphX HV-R Bone Cement
  • Modelo / Serial
    Model Catalog: 4-3000 (Lot serial: ); Model Catalog: 1-3216 (Lot serial: ); Model Catalog: 1-3014 (Lot serial: ); Model Catalog: 1-3006 (Lot serial: ); Model Catalog: 1-3010 (Lot serial: ); Model Catalog: 1-3008 (Lot serial: ); Model Catalog: 1-3012 (Lot serial: )
  • Descripción del producto
    X-STOP PEEK IPD SYSTEM

2 fabricantes con un nombre similar

Más información acerca de la data acá

  • Dirección del fabricante
    Medtronic Spine LLC, formerly Kyphon Inc, 1221 Crossman Ave, Sunnyvale CA 94089-1103
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    USFDA
  • Dirección del fabricante
    Medtronic Spine LLC (formerly Kyphon Inc.), 1221 Crossman Ave, Sunnyvale CA 94089-1103
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    USFDA