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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CoRoent® XL-W+, 8x22x55mm 10°
Nuvasive, Inc.
6308255
In Commercial Distribution

  • 00887517305428 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x50mm 10°
Nuvasive, Inc.
6308250
In Commercial Distribution

  • 00887517305411 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x45mm 10°
Nuvasive, Inc.
6308245
In Commercial Distribution

  • 00887517305404 ()


  • Polymeric spinal interbody fusion cage
Brigade Inserter, Medial Access Small
Nuvasive, Inc.
D7981214
In Commercial Distribution

  • 00887517305398 ()


  • Orthopaedic implant inserter/extractor, reusable
CoRoent® XL-W+, 8x22x40mm 10°
Nuvasive, Inc.
6308240
In Commercial Distribution

  • 00887517305091 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 10x22x60mm 30°
Nuvasive, Inc.
6301060
In Commercial Distribution

  • 00887517304384 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 10x22x55mm 30°
Nuvasive, Inc.
6301055
In Commercial Distribution

  • 00887517304377 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 10x22x50mm 30°
Nuvasive, Inc.
6301050
In Commercial Distribution

  • 00887517304360 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 10x22x45mm 30°
Nuvasive, Inc.
6301045
In Commercial Distribution

  • 00887517304353 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-H, 8x22x60mm 30°
Nuvasive, Inc.
6300860
In Commercial Distribution

  • 00887517304322 ()


  • Polymeric spinal interbody fusion cage
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