SPYDER Anastomotic Device

  • Model / Serial
    All units with Use Before Dates earlier than June, 2007.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Nationwide (AZ, CA, CT, FL, HI, IA, ID, IL, IN, KS, KY, LA, ,MD, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OK, PA, TN, TX, UT, WA, WI, WV). Japan, Belgium, Netherlands, Singapore, and Thailand.
  • Product Description
    Medtronic SPYDER Anastomotic Device. Sterilized using irradiation. Do not Reuse. Nonpyrogenic. The SPYDER is designed to create an anastomosis in a rapid, automated fashion. The device creates an interrupted anastomosis without the need for aortic clamping. A specially designed aortic cutting device (ACD) (sold separately) is utilized to create the site for the anastomosis.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Medtronic Cardiac Surgery Technologies, 7601 Northland Dr N, Minneapolis MN 55428-1088
  • Source
    USFDA