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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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Reform® Ti CT MIS Driver
PRECISION SPINE, INC.
70-CT-0750
In Commercial Distribution

  • 00840019975681 ()
70-CT-0750

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reform® Ti CT Polyaxial Driver
PRECISION SPINE, INC.
70-CT-0700
In Commercial Distribution

  • 00840019975674 ()
70-CT-0700

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reduction Driver, Cannulated
PRECISION SPINE, INC.
39-SP-1770
In Commercial Distribution

  • 00840019975667 ()
39-SP-1770

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reduction Driver
PRECISION SPINE, INC.
39-SP-0770
In Commercial Distribution

  • 00840019975650 ()
39-SP-0770

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reform® MAX Modular Driver BOM (GLOBOT)
PRECISION SPINE, INC.
73-BK-0105
In Commercial Distribution

  • 00840019973076 ()
73-BK-0105

  • Neurosurgical retraction system, spinal
Reform® MAX Modular Driver BOM (GLOBOT)
PRECISION SPINE, INC.
73-BK-0104
In Commercial Distribution

  • 00840019973069 ()
73-BK-0104

  • Neurosurgical retraction system, spinal
Reform® MAX Modular Driver BOM (GLOBOT)
PRECISION SPINE, INC.
73-BK-0103
In Commercial Distribution

  • 00840019973052 ()
73-BK-0103

  • Neurosurgical retraction system, spinal
Reform® MAX Modular Driver BOM (GLOBOT)
PRECISION SPINE, INC.
73-BK-0102
In Commercial Distribution

  • 00840019973045 ()
73-BK-0102

  • Spinal bone screw, non-bioabsorbable
Reform® MAX Modular Driver BOM (GLOBOT)
PRECISION SPINE, INC.
73-BK-0101
In Commercial Distribution

  • 00840019973038 ()
73-BK-0101

  • Neurosurgical retraction system, spinal
T20 Retractor Driver Assembly
PRECISION SPINE, INC.
73-IN-2085
In Commercial Distribution

  • 00840019972970 ()
73-IN-2085

  • Neurosurgical retraction system, spinal
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