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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ACP Driver, Angled Lock
Nuvasive, Inc.
8786788
In Commercial Distribution

  • 00887517014559 ()


  • Internal spinal fixation procedure kit, reusable
ACP Driver, Primary Lock Sleeve
Nuvasive, Inc.
8786786
In Commercial Distribution

  • 00887517014542 ()


  • Internal spinal fixation procedure kit, reusable
ACP 1.9H DTS Guide, 25° Double 2
Nuvasive, Inc.
8786770
In Commercial Distribution

  • 00887517014535 ()


  • Internal spinal fixation procedure kit, reusable
ACP 1.9H DTS Guide, 25° Double 1
Nuvasive, Inc.
8786767
In Commercial Distribution

  • 00887517014511 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Trial, 16x10mm 12°
Nuvasive, Inc.
3161012
In Commercial Distribution

  • 00887517014047 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Trial, 14x14mm 4°
Nuvasive, Inc.
3141404
In Commercial Distribution

  • 00887517014023 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Trial, 14x10mm 12°
Nuvasive, Inc.
3141012
In Commercial Distribution

  • 00887517014016 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Trial, 14x10mm 4°
Nuvasive, Inc.
3141004
In Commercial Distribution

  • 00887517014009 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Trial, 12x10mm 12°
Nuvasive, Inc.
3121012
In Commercial Distribution

  • 00887517013170 ()


  • Internal spinal fixation procedure kit, reusable
COHERE TLIF-O Trial, 11x10mm 8°
Nuvasive, Inc.
3111008
In Commercial Distribution

  • 00887517013156 ()


  • Internal spinal fixation procedure kit, reusable
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