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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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Titanium Interbody, 20 degree, 38mmx27mm
Altus Spine, LLC
SL38272015T
In Commercial Distribution

  • 00843210181103 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 38mmx27mm
Altus Spine, LLC
SL38272016T
In Commercial Distribution

  • 00843210181097 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 38mmx27mm
Altus Spine, LLC
SL38272017T
In Commercial Distribution

  • 00843210181080 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 38mmx27mm
Altus Spine, LLC
SL38272018T
In Commercial Distribution

  • 00843210181073 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 38mmx27mm
Altus Spine, LLC
SL38272019T
In Commercial Distribution

  • 00843210181066 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 38mmx27mm
Altus Spine, LLC
SL38272020T
In Commercial Distribution

  • 00843210181059 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 25 degree, 38mmx27mm
Altus Spine, LLC
SL38272516T
In Commercial Distribution

  • 00843210180618 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 25 degree, 38mmx27mm
Altus Spine, LLC
SL38272517T
In Commercial Distribution

  • 00843210180595 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 25 degree, 38mmx27mm
Altus Spine, LLC
SL38272518T
In Commercial Distribution

  • 00843210180571 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 25 degree, 38mmx27mm
Altus Spine, LLC
SL38272519T
In Commercial Distribution

  • 00843210180564 ()


  • Polymeric spinal interbody fusion cage
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