Device Recall Colorado 2 Anterior Plate

  • Model / Serial
    Lot Nos.: 42554, 59143, 74708, 076380, 076520, 81321, 82118, 82119, 82236, 83602, 83667, 98552, 177390, 177420, 229470, 230050, 365740, 662340, 685000, 857100, 877430, 909610, W05A1351, W05C5778, W05F5388, W05F5389, W05G1030, W05G2592, W05H1354, W05H7884, W05J1023, W05J1497, W05J1687, W05J2710, W05J2711, W05L0550, W05L1016, W06E3829, W06F4111, W06H1671, W06K1299, W06M1486, W06M1487.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    France, Germany, Italy, UK, and Tunisia. No US distribution.
  • Product Description
    Colorado 2 Spinal System, Anterior Plate, REF8639500, for export only, manufactured at: Warsaw, Indiana USA, Rx only
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Medtronic Sofamor Danek USA Inc, 1800 Pyramid Place, Memphis TN 38132-1719
  • Source
    USFDA

One device with a similar name

Learn more about the data here

  • Model / Serial
    Lot Nos.: W04E0149, W04C1938, 553880, 672660, 353150, 355610, 201190, 198840, 947250, 914870, 82549, 81749, 81320, 76967, 65867, 42841, 42842.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    France, Germany, Italy, UK, and Tunisia. No US distribution.
  • Product Description
    Colorado 2 Spinal System, Anterior Plate, REF8619500, for export only, manufactured at: Warsaw, Indiana USA, Rx only
  • Manufacturer