SEARCH RESULTS FOR: 太阳城集团注册送20→→1946.cc←←太阳城集团注册送20.zjmd(2996 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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CoRoent - 00887517822628

Interlock II Trial, 16x19x16mm 20° Stop
Nuvasive, Inc.
6773216
In Commercial Distribution

  • 00887517822628 ()


  • Spinal implant trial

CoRoent - 00887517822611

Interlock II Trial, 15x19x16mm 20° Stop
Nuvasive, Inc.
6773215
In Commercial Distribution

  • 00887517822611 ()


  • Spinal implant trial

CoRoent - 00887517822604

Interlock II Trial, 14x19x16mm 20° Stop
Nuvasive, Inc.
6773214
In Commercial Distribution

  • 00887517822604 ()


  • Spinal implant trial

CoRoent - 00887517822598

Interlock II Trial, 13x19x16mm 20° Stop
Nuvasive, Inc.
6773213
In Commercial Distribution

  • 00887517822598 ()


  • Spinal implant trial

CoRoent - 00887517822581

Interlock II Trial, 12x19x16mm 20° Stop
Nuvasive, Inc.
6773212
In Commercial Distribution

  • 00887517822581 ()


  • Spinal implant trial

CoRoent - 00887517822574

Interlock II Trial, 11x19x16mm 20° Stop
Nuvasive, Inc.
6773211
In Commercial Distribution

  • 00887517822574 ()


  • Spinal implant trial

CoRoent - 00887517822567

Interlock II Trial, 10x19x16mm 20° Stop
Nuvasive, Inc.
6773210
In Commercial Distribution

  • 00887517822567 ()


  • Spinal implant trial

CoRoent - 00887517822550

Interlock II Trial, 9x19x16mm 20° Stop
Nuvasive, Inc.
6773209
In Commercial Distribution

  • 00887517822550 ()


  • Spinal implant trial

Brickyard ALIF - 00843210184272

34mm x 26mm, 20°, 13mm PEEK Spacer
Altus Spine, LLC
FA34262013
In Commercial Distribution

  • 00843210184272 ()


  • Spinal implant trial

Brickyard ALIF - 00843210184258

34mm x 26mm, 20°, 13mm Ti Spacer
Altus Spine, LLC
FA34262013T
In Commercial Distribution

  • 00843210184258 ()


  • Spinal implant trial
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