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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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Torque Limiting Driver 95 in-lbs.
ORTHOPEDIATRICS CORP.
01-1300-0026
In Commercial Distribution

  • 00841132127995 ()
01-1300-0026

  • Surgical screwdriver, reusable
Angled Driver
ELEVATION SPINE, INC.
CI-ANG-DRIVER
In Commercial Distribution

  • 00810017914159 ()
CI-ANG-DRIVER

  • Internal spinal fixation procedure kit, single-use
Spike Driver, 10mm
ELEVATION SPINE, INC.
CI-DRIVER3-SP-10
In Commercial Distribution

  • 00810017913565 ()
CI-DRIVER3-SP-10

  • Internal spinal fixation procedure kit, single-use
Spike Driver, 8-9mm
ELEVATION SPINE, INC.
CI-DRIVER3-SP-89
In Commercial Distribution

  • 00810017913558 ()
CI-DRIVER3-SP-89

  • Internal spinal fixation procedure kit, single-use
Spike Driver, 5-7mm
ELEVATION SPINE, INC.
CI-DRIVER3-SP-567
In Commercial Distribution

  • 00810017913541 ()
CI-DRIVER3-SP-567

  • Internal spinal fixation procedure kit, single-use
Spike Driver, 10mm
ELEVATION SPINE, INC.
CI-DRIVER-SP-10
In Commercial Distribution

  • 00810017913244 ()
CI-DRIVER-SP-10

  • Internal spinal fixation procedure kit, single-use
Spike Driver, 8-9mm
ELEVATION SPINE, INC.
CI-DRIVER-SP-89
In Commercial Distribution

  • 00810017913237 ()
CI-DRIVER-SP-89

  • Internal spinal fixation procedure kit, single-use
Spike Driver, 5-7mm
ELEVATION SPINE, INC.
CI-DRIVER-SP-567
In Commercial Distribution

  • 00810017913220 ()
CI-DRIVER-SP-567

  • Internal spinal fixation procedure kit, single-use
Spike Driver (Final)
ELEVATION SPINE, INC.
CI-DRIVER-SPF
In Commercial Distribution

  • 00810017912391 ()
CI-DRIVER-SPF

  • Internal spinal fixation procedure kit, single-use
Spike Driver
ELEVATION SPINE, INC.
CI-DRIVER-SP
In Commercial Distribution

  • 00810017912384 ()
CI-DRIVER-SP

  • Internal spinal fixation procedure kit, single-use
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