Devices

Device Recall InterGro DBM Demineralized Bone Matrix

  • Modelo / Serial
    Lots 259990 and 318630 (exp 07/2009).
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    Class II Recall - Nationwide Distribution --- including the state of Michigan.
  • Descripción del producto
    InterGro DBM Demineralized Bone Matrix in a lipid carrier; Provided by: Lifelink Tissue Bank, Tampa, Florida, EBI A Biomet Company, Parsippany, New Jersey; REF DBM002. InterGro DBM product contain human tissue (allograft bpm) and are intended for transplantation. Products are to be used for filling bony voids or gaps in the extremities, and pelvis that are not intrinsic to the bony stability of the structure.
  • Manufacturer
    Michigan Orthopaedic Products, Inc.
  • 1 Event

Fabricante

Michigan Orthopaedic Products, Inc.
  • Dirección del fabricante
    Michigan Orthopaedic Products, Inc., 2905 Wilson Ave Sw Ste 100, Grandville MI 49418-1287
  • Source
    USFDA