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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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PROSPACE® - 04046963142216

PROSPACE PEEK IMPLANT 5° 13X10X25MM
Aesculap AG
SJ259P
Not in Commercial Distribution

  • 04046963142216 ()

  • Length : 25.000 MM
  • Height : 13.000 MM
  • Degree (°) : 5.000 DEG
SJ259P

  • Polymeric spinal interbody fusion cage

PROSPACE® - 04046963142209

PROSPACE PEEK IMPLANT 5° 11X10X25MM
Aesculap AG
SJ258P
Not in Commercial Distribution

  • 04046963142209 ()

  • Length : 25.000 MM
  • Height : 11.000 MM
  • Degree (°) : 5.000 DEG
SJ258P

  • Polymeric spinal interbody fusion cage

PROSPACE® - 04046963142193

PROSPACE PEEK IMPLANT 5° 9X8X22MM
Aesculap AG
SJ255P
Not in Commercial Distribution

  • 04046963142193 ()

  • Length : 22.000 MM
  • Degree (°) : 5.000 DEG
  • Height : 9.000 MM
SJ255P

  • Polymeric spinal interbody fusion cage

PROSPACE® - 04046963142186

PROSPACE PEEK IMPLANT 5° 7X8X22MM
Aesculap AG
SJ254P
Not in Commercial Distribution

  • 04046963142186 ()

  • Length : 22.000 MM
  • Degree (°) : 5.000 DEG
  • Height : 7.000 MM
SJ254P

  • Polymeric spinal interbody fusion cage

PROSPACE® - 04046963142179

PROSPACE PEEK IMPLANT 5° 9X8X19MM
Aesculap AG
SJ253P
Not in Commercial Distribution

  • 04046963142179 ()

  • Length : 19.000 MM
  • Degree (°) : 5.000 DEG
  • Height : 9.000 MM
SJ253P

  • Polymeric spinal interbody fusion cage

PROSPACE® - 04046963142131

PROSPACE PEEK IMPLANT 5° 9X10X22MM
Aesculap AG
SJ256P
Not in Commercial Distribution

  • 04046963142131 ()

  • Length : 22.000 MM
  • Degree (°) : 5.000 DEG
  • Height : 9.000 MM
SJ256P

  • Polymeric spinal interbody fusion cage

PROSPACE® - 04046963142070

PROSPACE PEEK IMPLANT 5° 7X8X19MM
Aesculap AG
SJ252P
Not in Commercial Distribution

  • 04046963142070 ()

  • Length : 19.000 MM
  • Degree (°) : 5.000 DEG
  • Height : 7.000 MM
SJ252P

  • Polymeric spinal interbody fusion cage

VEO® Lateral Interbody Fusion System - 00840996132244

ANTEROLATERAL,CURETTE,CUP,PUSH,#5
Choice Spine, LP
V070-0055
In Commercial Distribution

  • 00840996132244 ()


  • Polymeric spinal interbody fusion cage

VEO® Lateral Interbody Fusion System - 00840996132220

ANTEROLATERAL,CURETTE,CUP,PULL,#5
Choice Spine, LP
V070-0053
In Commercial Distribution

  • 00840996132220 ()


  • Polymeric spinal interbody fusion cage

VEO® Lateral Interbody Fusion System - 00840996132206

ANTEROLATERAL,CURETTE,CUP,STRAIGHT,#5
Choice Spine, LP
V070-0051
In Commercial Distribution

  • 00840996132206 ()


  • Polymeric spinal interbody fusion cage
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