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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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Cannulated Screw, 4.2 mm X 42 mm
Spine Wave, Inc.
21-8357
In Commercial Distribution

  • 10840642119930 ()
21-8357

  • Spinal bone screw, non-bioabsorbable
Cannulated Screw, 4.2 mm X 40 mm
Spine Wave, Inc.
21-8356
In Commercial Distribution

  • 10840642119923 ()
21-8356

  • Spinal bone screw, non-bioabsorbable
Cannulated Screw, 4.2 mm X 38 mm
Spine Wave, Inc.
21-8355
In Commercial Distribution

  • 10840642119916 ()
21-8355

  • Spinal bone screw, non-bioabsorbable
Cannulated Screw, 4.2 mm X 36 mm
Spine Wave, Inc.
21-8354
In Commercial Distribution

  • 10840642119909 ()
21-8354

  • Spinal bone screw, non-bioabsorbable
Cannulated Screw, 4.2 mm X 34 mm
Spine Wave, Inc.
21-8353
In Commercial Distribution

  • 10840642119893 ()
21-8353

  • Spinal bone screw, non-bioabsorbable
Cannulated Screw, 4.2 mm X 32 mm
Spine Wave, Inc.
21-8352
In Commercial Distribution

  • 10840642119886 ()
21-8352

  • Spinal bone screw, non-bioabsorbable
Cannulated Screw, 4.2 mm X 30 mm
Spine Wave, Inc.
21-8351
In Commercial Distribution

  • 10840642119879 ()
21-8351

  • Spinal bone screw, non-bioabsorbable
Cannulated Screw, 4.2 mm X 28 mm
Spine Wave, Inc.
21-8350
In Commercial Distribution

  • 10840642119862 ()
21-8350

  • Spinal bone screw, non-bioabsorbable
Cannulated Screw, 4.2 mm X 26 mm
Spine Wave, Inc.
21-8349
In Commercial Distribution

  • 10840642119855 ()
21-8349

  • Spinal bone screw, non-bioabsorbable
Cannulated Screw, 4.2 mm X 24 mm
Spine Wave, Inc.
21-8348
In Commercial Distribution

  • 10840642119848 ()
21-8348

  • Spinal bone screw, non-bioabsorbable
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