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

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Modulus-C Trial, 6x17x14mm 7°
Nuvasive, Inc.
Z700315-206
In Commercial Distribution

  • 00195377164612 ()


  • Internal spinal fixation procedure kit, reusable
Modulus-C Trial, 5x17x14mm 7°
Nuvasive, Inc.
Z700315-205
In Commercial Distribution

  • 00195377164605 ()


  • Internal spinal fixation procedure kit, reusable
VuePoint II Bender, Sagittal Angled Lt
Nuvasive, Inc.
Z700206-502
In Commercial Distribution

  • 00195377164599 ()


  • Internal spinal fixation procedure kit, reusable
VuePoint II Bender,Sagittal Angled Rt
Nuvasive, Inc.
Z700206-501
In Commercial Distribution

  • 00195377164582 ()


  • Internal spinal fixation procedure kit, reusable
VuePoint II Bender, Sagittal Right
Nuvasive, Inc.
Z700206-1
In Commercial Distribution

  • 00195377164568 ()


  • Internal spinal fixation procedure kit, reusable
Graft Funnel, 4.5mm Outer Diameter
Nuvasive, Inc.
Z900034-45
In Commercial Distribution

  • 00195377162212 ()


  • Internal spinal fixation procedure kit, reusable
ACP Driver, 6.35" Primary Lock Sleeve
Nuvasive, Inc.
Z700333-01
In Commercial Distribution

  • 00195377162205 ()


  • Internal spinal fixation procedure kit, reusable
RELINE C Tap, Ø3.0mm Sharp
Nuvasive, Inc.
Z700332-03
In Commercial Distribution

  • 00195377162199 ()


  • Internal spinal fixation procedure kit, reusable
RELINE Distractor, Intervertebral
Nuvasive, Inc.
Z500163
In Commercial Distribution

  • 00195377162182 ()


  • Internal spinal fixation procedure kit, reusable
MOD-EX PL Driver, Expansion Post Sleeve
Nuvasive, Inc.
Z500161-02
In Commercial Distribution

  • 00195377162168 ()


  • Internal spinal fixation procedure kit, reusable
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