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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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Zavation - 00842166181106

Retractor Blade 80 R
Zavation LLC
80-1059-080-R
In Commercial Distribution

  • 00842166181106 ()


  • Polymeric spinal interbody fusion cage

Zavation - 00842166181090

Retractor Blade 70 L
Zavation LLC
80-1059-070-L
In Commercial Distribution

  • 00842166181090 ()


  • Polymeric spinal interbody fusion cage

Zavation - 00842166181083

Retractor Blade 70 R
Zavation LLC
80-1059-070-R
In Commercial Distribution

  • 00842166181083 ()


  • Polymeric spinal interbody fusion cage

Zavation - 00842166181076

Retractor Blade 60 L
Zavation LLC
80-1059-060-L
In Commercial Distribution

  • 00842166181076 ()


  • Polymeric spinal interbody fusion cage

Zavation - 00842166181069

Retractor Blade 60 R
Zavation LLC
80-1059-060-R
In Commercial Distribution

  • 00842166181069 ()


  • Polymeric spinal interbody fusion cage

Zavation - 00842166181052

Retractor Blade 50 L
Zavation LLC
80-1059-050-L
In Commercial Distribution

  • 00842166181052 ()


  • Polymeric spinal interbody fusion cage

Zavation - 00842166181045

Retractor Blade 50 R
Zavation LLC
80-1059-050-R
In Commercial Distribution

  • 00842166181045 ()


  • Polymeric spinal interbody fusion cage

ZAVATION - 00842166181038

Central Blade Gen3
Zavation LLC
80-1058-210
In Commercial Distribution

  • 00842166181038 ()


  • Polymeric spinal interbody fusion cage

ZAVATION - 00842166181021

Central Blade Gen3
Zavation LLC
80-1058-200
In Commercial Distribution

  • 00842166181021 ()


  • Polymeric spinal interbody fusion cage

ZAVATION - 00842166181014

Central Blade Gen3
Zavation LLC
80-1058-190
In Commercial Distribution

  • 00842166181014 ()


  • Polymeric spinal interbody fusion cage
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