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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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PEEK/Titanium Interbody, 25 °, 42mm x 30mm
Altus Spine, LLC
SL42302520
In Commercial Distribution

  • 00843210188409 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 42mm x 30mm
Altus Spine, LLC
SL42302519
In Commercial Distribution

  • 00843210188393 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 42mm x 30mm
Altus Spine, LLC
SL42302518
In Commercial Distribution

  • 00843210188386 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 42mm x 30mm
Altus Spine, LLC
SL42302517
In Commercial Distribution

  • 00843210188379 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272520
In Commercial Distribution

  • 00843210188362 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272519
In Commercial Distribution

  • 00843210188355 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272518
In Commercial Distribution

  • 00843210188348 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272517
In Commercial Distribution

  • 00843210188331 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272516
In Commercial Distribution

  • 00843210188324 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272515
In Commercial Distribution

  • 00843210188317 ()


  • Polymeric spinal interbody fusion cage
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