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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 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-0104
In Commercial Distribution

  • 00840019973069 ()
73-BK-0104

  • Neurosurgical retraction system, spinal
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
T20 Blade Driver Assembly
PRECISION SPINE, INC.
73-IN-2075
In Commercial Distribution

  • 00840019972956 ()
73-IN-2075

  • Neurosurgical retraction system, spinal
Stab & Grab T25 Driver
PRECISION SPINE, INC.
73-SP-2600
In Commercial Distribution

  • 00840019972918 ()
73-SP-2600

  • Neurosurgical retraction system, spinal
Stab & Grab T25 Driver - NAV
PRECISION SPINE, INC.
70-SP-2600
In Commercial Distribution

  • 00840019972895 ()
70-SP-2600

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Modular T25 Driver - NAV
PRECISION SPINE, INC.
70-MD-2800
In Commercial Distribution

  • 00840019972888 ()
70-MD-2800

  • Orthopaedic surgical procedure kit, non-medicated, reusable
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