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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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SQUARE CONNECT DRIVER SHAFT, T-LIFT, 14 DEG
SPINEFRONTIER, INC.
14-05005
In Commercial Distribution

  • 00190361023210 ()


  • Polymeric spinal interbody fusion cage
DRIVER SILK SCREW 1.5MM
Smith & Nephew, Inc.
014815
In Commercial Distribution

  • 03596010026477 ()
014815

  • Orthopaedic implant driver
DRVR FIXATION POST W/HLDR.
Smith & Nephew, Inc.
013124
In Commercial Distribution

  • 03596010024664 ()
013124

  • Orthopaedic implant driver
Polyaxial Driver
PRECISION SPINE, INC.
39-SP-0720
In Commercial Distribution

  • 00840019929172 ()
39-SP-0720

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Retention Bone-Screw Driver
PRECISION SPINE, INC.
39-SP-0610
In Commercial Distribution

  • 00840019929165 ()
39-SP-0610

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Driver with Mechanical Lock
PRECISION SPINE, INC.
HXX-39-0001
In Commercial Distribution

  • 00840019928809 ()
HXX-39-0001

  • Orthopaedic surgical procedure kit, non-medicated, reusable
MIS Polyaxial Screw Driver
PRECISION SPINE, INC.
39-SP-0710
In Commercial Distribution

  • 00840019928748 ()
39-SP-0710

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Polyaxial Driver
PRECISION SPINE, INC.
39-SP-0700
In Commercial Distribution

  • 00840019928731 ()
39-SP-0700

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Dual-Side Lock Screw Driver
PRECISION SPINE, INC.
39-SP-0603
In Commercial Distribution

  • 00840019928724 ()
39-SP-0603

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Lock Screw Retention Driver
PRECISION SPINE, INC.
39-SP-0602
In Commercial Distribution

  • 00840019928717 ()
39-SP-0602

  • Orthopaedic surgical procedure kit, non-medicated, reusable
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