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 Class Implantable

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MOD-EX XLIF, 12x22x60mm 10-25° HL
Nuvasive, Inc.
5022601P2
In Commercial Distribution

  • 00195377061744 ()


  • Metallic spinal interbody fusion cage
MOD-EX XLIF, 12x22x45mm 10-25° HL
Nuvasive, Inc.
5022451P2
In Commercial Distribution

  • 00195377061737 ()


  • Metallic spinal interbody fusion cage
XLIF AMS Crestline Inserter, 15°
Nuvasive, Inc.
2775915
In Commercial Distribution

  • 00195377061515 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Removal Tool
Nuvasive, Inc.
1814379
In Commercial Distribution

  • 00195377056993 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Inserter, 14mm Impaction
Nuvasive, Inc.
D1814394
In Commercial Distribution

  • 00195377056986 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Inserter, 10mm Impaction
Nuvasive, Inc.
D1814390
In Commercial Distribution

  • 00195377056979 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Inserter, 10mm Long
Nuvasive, Inc.
D1814387
In Commercial Distribution

  • 00195377056962 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Inserter, 10mm
Nuvasive, Inc.
D1814386
In Commercial Distribution

  • 00195377056955 ()


  • Internal spinal fixation procedure kit, reusable
MOD-EX XLIF, 8x18x60mm 0-15°
Nuvasive, Inc.
5088600P2
In Commercial Distribution

  • 00195377056238 ()


  • Metallic spinal interbody fusion cage
MOD-EX XLIF, 8x18x55mm 0-15°
Nuvasive, Inc.
5088550P2
In Commercial Distribution

  • 00195377056221 ()


  • Metallic spinal interbody fusion cage
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