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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 Class Implantable

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XLIF - 00887517022370

XLIF AMS Inserter, Angled
Nuvasive, Inc.
1775950
In Commercial Distribution

  • 00887517022370 ()


  • Internal spinal fixation procedure kit, reusable

Cohere - 00887517020857

COHERE TLIF-O, 14x10x30mm 4°
Nuvasive, Inc.
6140304P2
In Commercial Distribution

  • 00887517020857 ()


  • Polymeric spinal interbody fusion cage

Cohere - 00887517020840

COHERE TLIF-O, 14x10x30mm 12°
Nuvasive, Inc.
6140302P2
In Commercial Distribution

  • 00887517020840 ()


  • Polymeric spinal interbody fusion cage

Cohere - 00887517020833

COHERE TLIF-O, 14x10x25mm 4°
Nuvasive, Inc.
6140254P2
In Commercial Distribution

  • 00887517020833 ()


  • Polymeric spinal interbody fusion cage

Cohere - 00887517020826

COHERE TLIF-O, 14x10x25mm 12°
Nuvasive, Inc.
6140252P2
In Commercial Distribution

  • 00887517020826 ()


  • Polymeric spinal interbody fusion cage

Cohere - 00887517020819

COHERE TLIF-O, 12x10x35mm 4°
Nuvasive, Inc.
6120354P2
In Commercial Distribution

  • 00887517020819 ()


  • Polymeric spinal interbody fusion cage

Cohere - 00887517020802

COHERE TLIF-O, 12x10x30mm 4°
Nuvasive, Inc.
6120304P2
In Commercial Distribution

  • 00887517020802 ()


  • Polymeric spinal interbody fusion cage

Cohere - 00887517020796

COHERE TLIF-O, 12x10x30mm 12°
Nuvasive, Inc.
6120302P2
In Commercial Distribution

  • 00887517020796 ()


  • Polymeric spinal interbody fusion cage

Cohere - 00887517020789

COHERE TLIF-O, 12x10x25mm 4°
Nuvasive, Inc.
6120254P2
In Commercial Distribution

  • 00887517020789 ()


  • Polymeric spinal interbody fusion cage

Cohere - 00887517020772

COHERE TLIF-O, 12x10x25mm 12°
Nuvasive, Inc.
6120252P2
In Commercial Distribution

  • 00887517020772 ()


  • Polymeric spinal interbody fusion cage
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