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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VuePoint Drill Bit, 2.05mm
Nuvasive, Inc.
7907014
In Commercial Distribution

  • 00887517104632 ()


  • Internal spinal fixation procedure kit, single-use
VuePoint Template, 45mm Keel Plate
Nuvasive, Inc.
7907346
In Commercial Distribution

  • 00887517104625 ()


  • Internal spinal fixation procedure kit, single-use
VuePoint Template, 40mm Keel Plate
Nuvasive, Inc.
7907341
In Commercial Distribution

  • 00887517104618 ()


  • Internal spinal fixation procedure kit, single-use
VuePoint Template, 35mm Keel Plate
Nuvasive, Inc.
7907336
In Commercial Distribution

  • 00887517104601 ()


  • Internal spinal fixation procedure kit, single-use
MAXCESS IV 12MM CENTER BLADE ASSEMBLY 15
Nuvasive, Inc.
1552629
In Commercial Distribution

  • 00887517104595 ()


  • Surgical retraction system, reusable
MAXCESS IV 12MM CENTER BLADE ASSEMBLY 14
Nuvasive, Inc.
1552628
In Commercial Distribution

  • 00887517104588 ()


  • Surgical retraction system, reusable
MAXCESS IV 12MM CENTER BLADE ASSEMBLY 13
Nuvasive, Inc.
1552627
In Commercial Distribution

  • 00887517104571 ()


  • Surgical retraction system, reusable
MAXCESS IV 12MM CENTER BLADE ASSEMBLY 12
Nuvasive, Inc.
1552626
In Commercial Distribution

  • 00887517104564 ()


  • Surgical retraction system, reusable
MAXCESS IV 12MM CENTER BLADE ASSEMBLY 11
Nuvasive, Inc.
1552625
In Commercial Distribution

  • 00887517104557 ()


  • Surgical retraction system, reusable
MAXCESS IV 12MM CENTER BLADE ASSEMBLY 10
Nuvasive, Inc.
1552624
In Commercial Distribution

  • 00887517104540 ()


  • Surgical retraction system, reusable
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