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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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Screw Retention Driver - T10
PRECISION SPINE, INC.
65-IN-0730
In Commercial Distribution

  • 00840019937948 ()
65-IN-0730

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reduction Locking Polyaxial Driver
PRECISION SPINE, INC.
39-SP-0740
In Commercial Distribution

  • 00840019935890 ()
39-SP-0740

  • Orthopaedic surgical procedure kit, non-medicated, reusable
T25 SELF RETAINING DRIVER, CANNULATED
ALPHATEC SPINE, INC.
87713
In Commercial Distribution

  • 00190376054674 ()


  • Surgical screwdriver, reusable
Cannulated Reduction Polyaxial Screw Driver, NI
ALPHATEC SPINE, INC.
87781
In Commercial Distribution

  • 00190376003702 ()


  • Surgical screwdriver, reusable
Cannulated Polyaxial Screw Driver, NI
ALPHATEC SPINE, INC.
87778
In Commercial Distribution

  • 00190376003337 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reduction Polyaxial Screw Driver, NI
ALPHATEC SPINE, INC.
87772
In Commercial Distribution

  • 00190376002996 ()


  • Surgical screwdriver, reusable
Polyaxial Screw Driver, NI
ALPHATEC SPINE, INC.
87771
In Commercial Distribution

  • 00190376002965 ()


  • Surgical screwdriver, reusable
Reduction Polyaxial Screw Driver, NI
ALPHATEC SPINE, INC.
73768
In Commercial Distribution

  • 00190376002521 ()


  • Surgical screwdriver, reusable
Polyaxial Screw Driver, NI
ALPHATEC SPINE, INC.
73767
In Commercial Distribution

  • 00190376002484 ()


  • Surgical screwdriver, reusable
Cannulated Polyaxial Driver
PRECISION SPINE, INC.
39-SP-0750
In Commercial Distribution

  • 00840019932455 ()
39-SP-0750

  • Orthopaedic surgical procedure kit, non-medicated, reusable
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