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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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ReLine - 00195377080943

RELINE C Driver,Counter Torque Occip Ang
Nuvasive, Inc.
3995006
In Commercial Distribution

  • 00195377080943 ()


  • Internal spinal fixation procedure kit, reusable

ReLine - 00195377080578

RELINE C Driver, Hex Nut
Nuvasive, Inc.
3990047
In Commercial Distribution

  • 00195377080578 ()


  • Internal spinal fixation procedure kit, reusable

ReLine - 00195377080448

RELINE C Driver, Spoke
Nuvasive, Inc.
3990027
In Commercial Distribution

  • 00195377080448 ()


  • Internal spinal fixation procedure kit, reusable

ReLine - 00195377080356

RELINE C Driver, Final Tightening
Nuvasive, Inc.
3990016
In Commercial Distribution

  • 00195377080356 ()


  • Internal spinal fixation procedure kit, reusable

ReLine - 00195377080325

RELINE C Driver, Tapered
Nuvasive, Inc.
3990012
In Commercial Distribution

  • 00195377080325 ()


  • Internal spinal fixation procedure kit, reusable

ReLine - 00195377080318

RELINE C Driver, Stab-n-Grab
Nuvasive, Inc.
3990011
In Commercial Distribution

  • 00195377080318 ()


  • Internal spinal fixation procedure kit, reusable

ACP - 00195377029102

ACP Driver, Temporary Fixation Pin
Nuvasive, Inc.
D7786704
In Commercial Distribution

  • 00195377029102 ()


  • Internal spinal fixation procedure kit, reusable

ACP - 00195377029096

ACP Driver, Ball Hex
Nuvasive, Inc.
7786735
In Commercial Distribution

  • 00195377029096 ()


  • Internal spinal fixation procedure kit, reusable

ACP - 00195377029089

ACP Driver, Screw Retention
Nuvasive, Inc.
7786730
In Commercial Distribution

  • 00195377029089 ()


  • Internal spinal fixation procedure kit, reusable

ACP - 00195377029072

ACP Driver, Screw and Lock Tapered
Nuvasive, Inc.
7786729
In Commercial Distribution

  • 00195377029072 ()


  • Internal spinal fixation procedure kit, reusable
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