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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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IdentiTi II - 00190376599717

ID II PC, INTRADISCAL DISTRACTOR TIP, 6mm
ALPHATEC SPINE, INC.
823-500-06
In Commercial Distribution

  • 00190376599717 ()


  • Bone lever/elevator, reusable

IdentiTi II - 00190376599700

ID II PC, INTRADISCAL DISTRACTOR TIP, 5mm
ALPHATEC SPINE, INC.
823-500-05
In Commercial Distribution

  • 00190376599700 ()


  • Bone lever/elevator, reusable

IdentiTi II - 00190376599694

ID II TLIF-A, CURVED BOX CUTTER 7mm
ALPHATEC SPINE, INC.
823-300-07
In Commercial Distribution

  • 00190376599694 ()


  • Bone cutter

IdentiTi II - 00190376595719

ID II TLIF-A, CURVED BOX CUTTER 10mm
ALPHATEC SPINE, INC.
823-300-10
In Commercial Distribution

  • 00190376595719 ()


  • Bone cutter

IdentiTi II - 00190376595702

ID II TLIF-A, CURVED BOX CUTTER 9mm
ALPHATEC SPINE, INC.
823-300-09
In Commercial Distribution

  • 00190376595702 ()


  • Bone cutter

IdentiTi II - 00190376595696

ID II TLIF-A, CURVED BOX CUTTER 8mm
ALPHATEC SPINE, INC.
823-300-08
In Commercial Distribution

  • 00190376595696 ()


  • Bone cutter

IdentiTi II - 00190376595689

ID II TLIF-A, CURVED BOX CUTTER 6mm
ALPHATEC SPINE, INC.
823-300-06
In Commercial Distribution

  • 00190376595689 ()


  • Bone cutter

IdentiTi II - 00190376595672

ID II TLIF-A, CURVED BOX CUTTER 5mm
ALPHATEC SPINE, INC.
823-300-05
In Commercial Distribution

  • 00190376595672 ()


  • Bone cutter

IdentiTi II - 00190376595665

ID II TLIF-A, CURVED BOX CUTTER 4mm
ALPHATEC SPINE, INC.
823-300-04
In Commercial Distribution

  • 00190376595665 ()


  • Bone cutter

SLR BIPOLAR - M684170032121

SLR BIPOLAR INSERT 63-65mm X 32mm ID
Microport Orthopedics Inc.
17003212
In Commercial Distribution

  • 17003212 ()
  • M684170032121 ()

  • Lumen/Inner Diameter: 32 Millimeter
17003212

  • Bipolar femoral head outer component, hemiarthroplasty
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