Devices

Device Recall ProPlan CMF

  • Model / Serial
    Item reference SD900.106; Unique Instrument ID MC13-OVA-OGO_01
  • Distribution
    Distributed in Canada.
  • Product Description
    ProPlan CMF Guide(s) Model(s) || REF SD900.008 Description: Single Use Only : Patient-Specific Guide, Orthognathic, Intermediate Single Use Only Rx only. || Used as surgical tools to transfer a pre-operative plan to surgery.
  • Manufacturer
    Materialise USA LLC
  • 1 Event

Manufacturer

Materialise USA LLC
  • Manufacturer Address
    Materialise USA LLC, 44650 Helm Ct, Plymouth MI 48170-6061
  • Manufacturer Parent Company (2017)
    Materialise Nv
  • Source
    USFDA

One device with a similar name

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Device Recall ProPlan CMF
  • Model / Serial
    Item reference SD900.106; Unique Instrument ID MC13-OVA-OGO_2
  • Distribution
    Distributed in Canada.
  • Product Description
    ProPlan CMF Guide(s) Model(s) || REF SD900.008 Description: Single Use Only : Patient-Specific Guide, Orthognathic, Final Single Use Only Rx only. || Used as surgical tools to transfer a pre-operative plan to surgery. || .
  • Manufacturer
    Materialise USA LLC