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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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Evolution Revision CCK System - M684EIK4S24L1

No Description
Microport Orthopedics Inc.
EIK4S24L
In Commercial Distribution

  • M684EIK4S24L1 ()

  • Thickness 24 mm
EIK4S24L

  • Tibial insert

Evolution Revision CCK System - M684EIK3S24R1

No Description
Microport Orthopedics Inc.
EIK3S24R
In Commercial Distribution

  • M684EIK3S24R1 ()

  • Thickness 24 mm
EIK3S24R

  • Tibial insert

Evolution Revision CCK System - M684EIK3S24L1

No Description
Microport Orthopedics Inc.
EIK3S24L
In Commercial Distribution

  • M684EIK3S24L1 ()

  • Thickness 24 mm
EIK3S24L

  • Tibial insert

Evolution Revision CCK System - M684EIK2S24R1

No Description
Microport Orthopedics Inc.
EIK2S24R
In Commercial Distribution

  • M684EIK2S24R1 ()

  • Thickness 24 mm
EIK2S24R

  • Tibial insert

Evolution Revision CCK System - M684EIK2S24L1

No Description
Microport Orthopedics Inc.
EIK2S24L
In Commercial Distribution

  • M684EIK2S24L1 ()

  • Thickness 24 mm
EIK2S24L

  • Tibial insert

Evolution Revision CCK System - M684EIK2P24R1

No Description
Microport Orthopedics Inc.
EIK2P24R
In Commercial Distribution

  • M684EIK2P24R1 ()

  • Thickness 24 mm
EIK2P24R

  • Tibial insert

Evolution Revision CCK System - M684EIK2P24L1

No Description
Microport Orthopedics Inc.
EIK2P24L
In Commercial Distribution

  • M684EIK2P24L1 ()

  • Thickness 24 mm
EIK2P24L

  • Tibial insert

Evolution Revision CCK System - M684EIK1S24R1

No Description
Microport Orthopedics Inc.
EIK1S24R
In Commercial Distribution

  • M684EIK1S24R1 ()

  • Thickness 24 mm
EIK1S24R

  • Tibial insert

Evolution Revision CCK System - M684EIK1S24L1

No Description
Microport Orthopedics Inc.
EIK1S24L
In Commercial Distribution

  • M684EIK1S24L1 ()

  • Thickness 24 mm
EIK1S24L

  • Tibial insert

Auragen™ - 10381780035312

The AURAGEN™ Cortical Surface Electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are placed on the exposed cortical surface or inserted into the subdural space to contact the cortical surface. Cortical Electrodes are available with platinum contacts and vary in size according to the number of contacts. The type of cortical electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
40M85
Not in Commercial Distribution

  • M27240M851 ()
  • 10381780035312 ()

  • 24 platinum contacts


  • Cortical electrode
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