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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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Bullnose Trial 23mm X 12mm X 55mm, 10°
Seaspine Orthopedics Corporation
SR-1288-431210
In Commercial Distribution

  • 10889981331429 ()
SR-1288-431210

  • Spinal implant trial
Bullnose Trial 18mm X 14mm X 55mm, 15°
Seaspine Orthopedics Corporation
SR-1288-381415
In Commercial Distribution

  • 10889981331405 ()
SR-1288-381415

  • Spinal implant trial
Bullnose Trial 18mm X 12mm X 55mm, 15°
Seaspine Orthopedics Corporation
SR-1288-381215
In Commercial Distribution

  • 10889981331382 ()
SR-1288-381215

  • Spinal implant trial
Bullnose Trial 18mm X 10mm X 55mm, 15°
Seaspine Orthopedics Corporation
SR-1288-381015
In Commercial Distribution

  • 10889981331375 ()
SR-1288-381015

  • Spinal implant trial
Bullnose Trial 18mm X 12mm X 55mm, 10°
Seaspine Orthopedics Corporation
SR-1288-381210
In Commercial Distribution

  • 10889981331368 ()
SR-1288-381210

  • Spinal implant trial
Bullnose Trial 18mm X 8mm X 55mm, 10°
Seaspine Orthopedics Corporation
SR-1288-380810
In Commercial Distribution

  • 10889981331344 ()
SR-1288-380810

  • Spinal implant trial
ALIF Starter Trial, 31mmx24mmx7mm, Up Angled
Seaspine Orthopedics Corporation
SR-1291
In Commercial Distribution

  • 10889981331207 ()
SR-1291

  • Spinal implant trial
ALIF Starter Trial, 31mmx24mmx7mm, Straight
Seaspine Orthopedics Corporation
SR-1290
In Commercial Distribution

  • 10889981331191 ()
SR-1290

  • Spinal implant trial
Lollipop Trial, Anterior-Angled, 23mm x 14mm x 55mm, 15°
Seaspine Orthopedics Corporation
SR-1249-2314-15
In Commercial Distribution

  • 10889981331085 ()
SR-1249-2314-15

  • Spinal implant trial
Lollipop Trial, Anterior-Angled, 23mm x 14mm x 55mm, 10°
Seaspine Orthopedics Corporation
SR-1249-2314-10
In Commercial Distribution

  • 10889981331078 ()
SR-1249-2314-10

  • Spinal implant trial
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