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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TRIAL 5251120 L 25 HT 11 DEG 20 ART
MEDTRONIC SOFAMOR DANEK, INC.
5251120
In Commercial Distribution

  • 00763000086046 ()


  • Spinal implant trial
TRIAL 5251020 L 25 HT 10 DEG 20 ART
MEDTRONIC SOFAMOR DANEK, INC.
5251020
In Commercial Distribution

  • 00763000086039 ()


  • Spinal implant trial
TRIAL 5251320 L 25 HT 13 DEG 20 ART
MEDTRONIC SOFAMOR DANEK, INC.
5251320
In Commercial Distribution

  • 00763000086060 ()


  • Spinal implant trial
TRIAL 5251220 L 25 HT 12 DEG 20 ART
MEDTRONIC SOFAMOR DANEK, INC.
5251220
In Commercial Distribution

  • 00763000086053 ()


  • Spinal implant trial
38mm x 27mm, 20°, 20mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38272020
In Commercial Distribution

  • 00843210140681 ()


  • Spinal implant trial
38mm x 27mm, 20°, 18mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38272018
In Commercial Distribution

  • 00843210140674 ()


  • Spinal implant trial
38mm x 27mm, 20°, 16mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38272016
In Commercial Distribution

  • 00843210140667 ()


  • Spinal implant trial
38mm x 27mm, 20°, 14mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38272014
In Commercial Distribution

  • 00843210140650 ()


  • Spinal implant trial
38mm x 27mm, 20°, 14mm Ti Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38272014T
In Commercial Distribution

  • 00843210139692 ()


  • Spinal implant trial
34mm x 26mm, 20°, 20mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA34262020
In Commercial Distribution

  • 00843210128535 ()


  • Spinal implant trial
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