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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MAS Midline Trial, M
Nuvasive, Inc.
1809622
In Commercial Distribution

  • 00887517709486 ()


  • Lumbar interspinous decompression instrument set, reusable
MAS Midline Trial, S
Nuvasive, Inc.
1809621
In Commercial Distribution

  • 00887517709479 ()


  • Lumbar interspinous decompression instrument set, reusable
BASE Driver, Straight
Nuvasive, Inc.
D6957000
In Commercial Distribution

  • 00887517709318 ()


  • Surgical screwdriver, reusable
MaXcess MAS TLIF Lateral Shim, Right
Nuvasive, Inc.
1680143
In Commercial Distribution

  • 00887517709264 ()


  • Orthopaedic surgical procedure kit, non-medicated, single-use
MaXcess MAS TLIF Lateral Shim, Left
Nuvasive, Inc.
1680142
In Commercial Distribution

  • 00887517709257 ()


  • Orthopaedic surgical procedure kit, non-medicated, single-use
BASE Centering Pin
Nuvasive, Inc.
6950099
In Commercial Distribution

  • 00887517707512 ()


  • External spinal fixation system
GDS Tube, Tapered Small
Nuvasive, Inc.
5120961
In Commercial Distribution

  • 00887517707505 ()


  • Surgical/emergency suction cannula, non-illuminating, reusable
GDS Applicator, Ø5mm Threaded
Nuvasive, Inc.
5120941
In Commercial Distribution

  • 00887517707499 ()


  • Neurosurgical procedure kit, non-medicated, reusable
GDS Tube, 8.4mm Curved
Nuvasive, Inc.
5120931
In Commercial Distribution

  • 00887517707482 ()


  • Surgical/emergency suction cannula, non-illuminating, reusable
GDS Tube, 7.5mm Curved
Nuvasive, Inc.
5120930
In Commercial Distribution

  • 00887517707475 ()


  • Surgical/emergency suction cannula, non-illuminating, reusable
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