SEARCH RESULTS FOR: 得克萨斯A(34825 results)

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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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Indy - 00843210140711

38mm x 27mm, 25°, 20mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38272520
In Commercial Distribution

  • 00843210140711 ()


  • Spinal implant trial

Indy - 00843210140704

38mm x 27mm, 25°, 18mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38272518
In Commercial Distribution

  • 00843210140704 ()


  • Spinal implant trial

Indy - 00843210140698

38mm x 27mm, 25°, 16mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38272516
In Commercial Distribution

  • 00843210140698 ()


  • Spinal implant trial

Indy - 00843210140681

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

  • 00843210140681 ()


  • Spinal implant trial

Indy - 00843210140674

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

  • 00843210140674 ()


  • Spinal implant trial

Indy - 00843210140667

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

  • 00843210140667 ()


  • Spinal implant trial

Indy - 00843210140650

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

  • 00843210140650 ()


  • Spinal implant trial

Indy - 00843210140643

38mm x 27mm, 16°, 20mmPEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38271620
In Commercial Distribution

  • 00843210140643 ()


  • Spinal implant trial

Indy - 00843210140636

38mm x 27mm, 16°, 18mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38271618
In Commercial Distribution

  • 00843210140636 ()


  • Spinal implant trial

Indy - 00843210140629

38mm x 27mm, 16°, 16mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA38271616
In Commercial Distribution

  • 00843210140629 ()


  • Spinal implant trial
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