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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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SureMAX-SA - 00817662024752

SureMAX-SA — 7° Small 5
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662024752 ()
1022-07121405

  • Metallic spinal interbody fusion cage

SureMAX-SA - 00817662025780

AWL GUIDE SIZE 5
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662025780 ()
1022-502

  • Metallic spinal interbody fusion cage

Modulus - 00887517828996

Modulus XLXW, 8x26x60mm 5°
Nuvasive, Inc.
1263860P2
In Commercial Distribution

  • 00887517828996 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517828972

Modulus XLXW, 8x26x55mm 5°
Nuvasive, Inc.
1263855P2
In Commercial Distribution

  • 00887517828972 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517828958

Modulus XLXW, 8x26x50mm 5°
Nuvasive, Inc.
1263850P2
In Commercial Distribution

  • 00887517828958 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517828934

Modulus XLXW, 8x26x45mm 5°
Nuvasive, Inc.
1263845P2
In Commercial Distribution

  • 00887517828934 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517828750

Modulus XLW, 8x22x60mm 5°
Nuvasive, Inc.
1223860P2
In Commercial Distribution

  • 00887517828750 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517828736

Modulus XLW, 8x22x55mm 5°
Nuvasive, Inc.
1223855P2
In Commercial Distribution

  • 00887517828736 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517828712

Modulus XLW, 8x22x50mm 5°
Nuvasive, Inc.
1223850P2
In Commercial Distribution

  • 00887517828712 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517828699

Modulus XLW, 8x22x45mm 5°
Nuvasive, Inc.
1223845P2
In Commercial Distribution

  • 00887517828699 ()


  • Metallic spinal interbody fusion cage
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