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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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4 Level, 74mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporary stabilization to the anterior spine during the development of cervical spine fusions (C2-T1) for the following indications: degenerative disc disease (DDD) (defined as neck pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion.
MEDICAL DESIGNS LLC
11-1106-FD4-74
In Commercial Distribution

  • 111106474 ()
  • M364111106FD4740 ()


  • Spinal fixation plate, non-bioabsorbable
3 Level, 75mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporary stabilization to the anterior spine during the development of cervical spine fusions (C2-T1) for the following indications: degenerative disc disease (DDD) (defined as neck pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion.
MEDICAL DESIGNS LLC
11-1106-FD3-75
In Commercial Distribution

  • 111106375 ()
  • M364111106FD3750 ()


  • Spinal fixation plate, non-bioabsorbable
3 Level, 72mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporary stabilization to the anterior spine during the development of cervical spine fusions (C2-T1) for the following indications: degenerative disc disease (DDD) (defined as neck pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion.
MEDICAL DESIGNS LLC
11-1106-FD3-72
In Commercial Distribution

  • 111106372 ()
  • M364111106FD3720 ()


  • Spinal fixation plate, non-bioabsorbable
Self-Drilling Screw - Low-Profile - Ø1.5mm x 5 mm [5 PK]
Bioplate, Inc.
81-5742[US]
In Commercial Distribution

  • M384815742US1 ()
  • M384815742US0 ()

  • Length: 5 Millimeter
81-5742[US]

  • Craniofacial bone screw, non-bioabsorbable
Self-Drilling Screw - Low-Profile - Ø1.5mm x 5 mm [5 PK]
Bioplate, Inc.
81-5742
In Commercial Distribution

  • M3848157421 ()
  • M3848157420 ()

  • Length: 5 Millimeter
81-5742

  • Craniofacial bone screw, non-bioabsorbable
Self-Drilling Screw - Low-Profile - Ø1.5mm x 4 mm [5 PK]
Bioplate, Inc.
81-5741[US]
In Commercial Distribution

  • M384815741US1 ()
  • M384815741US0 ()

  • Length: 4 Millimeter
81-5741[US]

  • Craniofacial bone screw, non-bioabsorbable
Self-Drilling Screw - Low-Profile - Ø1.5mm x 4 mm [5 PK]
Bioplate, Inc.
81-5741
In Commercial Distribution

  • M3848157411 ()
  • M3848157410 ()

  • Length: 4 Millimeter
81-5741

  • Craniofacial bone screw, non-bioabsorbable
Self-Drilling Screw - Low-Profile - Ø1.5mm x 3 mm [5 PK]
Bioplate, Inc.
81-5740[US]
In Commercial Distribution

  • M384815740US1 ()
  • M384815740US0 ()

  • Length: 3 Millimeter
81-5740[US]

  • Craniofacial bone screw, non-bioabsorbable
Self-Drilling Screw - Low-Profile - Ø1.5mm x 3 mm [5 PK]
Bioplate, Inc.
81-5740
In Commercial Distribution

  • M3848157401 ()
  • M3848157400 ()

  • Length: 3 Millimeter
81-5740

  • Craniofacial bone screw, non-bioabsorbable
Self-Drilling Screw - Low-Profile - Ø1.5mm x 3 mm [50 PK]
Bioplate, Inc.
81-3521
In Commercial Distribution

  • M3848135211 ()
  • M3848135210 ()

  • Length: 3 Millimeter
81-3521

  • Craniofacial bone screw, non-bioabsorbable
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