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 Class Implantable

Show Filters

Modulus ALIF Trial Rasp, 12x42x32 25°
Nuvasive, Inc.
1300196
In Commercial Distribution

  • 00195377050908 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial Rasp, 10x42x32mm 2
Nuvasive, Inc.
1300195
In Commercial Distribution

  • 00195377050892 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial Rasp, 8x42x32mm 25
Nuvasive, Inc.
1300194
In Commercial Distribution

  • 00195377050885 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial Rasp, 6x42x32mm 25
Nuvasive, Inc.
1300193
In Commercial Distribution

  • 00195377050878 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 12x42x32mm 20°
Nuvasive, Inc.
1300192
In Commercial Distribution

  • 00195377050861 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 10x42x32mm 20°
Nuvasive, Inc.
1300191
In Commercial Distribution

  • 00195377050854 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 8x42x32mm 20° L
Nuvasive, Inc.
1300190
In Commercial Distribution

  • 00195377050847 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 6x42x32mm 20° L
Nuvasive, Inc.
1300189
In Commercial Distribution

  • 00195377050830 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 12x42x32mm 15°
Nuvasive, Inc.
1300188
In Commercial Distribution

  • 00195377050823 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 10x42x32mm 15°
Nuvasive, Inc.
1300187
In Commercial Distribution

  • 00195377050816 ()


  • Internal spinal fixation procedure kit, reusable
< 1 ... 452 453 454 455 456 ... 486 >