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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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42X 30X 15mm X 20° PEEK
PRECISION SPINE, INC.
69-AV-2015
In Commercial Distribution

  • 00840019962681 ()
69-AV-2015

  • Polymeric spinal interbody fusion cage
42X 30X 13mm X 20° PEEK
PRECISION SPINE, INC.
69-AV-2013
In Commercial Distribution

  • 00840019962674 ()
69-AV-2013

  • Polymeric spinal interbody fusion cage
7 X 20 MM BIORCI SCREW
Smith & Nephew, Inc.
7207916
In Commercial Distribution

  • 03596010000897 ()
7207916

  • Bioabsorbable orthopaedic bone screw
9 X 20 MM BIORCI SCREW
Smith & Nephew, Inc.
7207919
In Commercial Distribution

  • 03596010485557 ()
7207919

  • Bioabsorbable orthopaedic bone screw
8 X 20 MM BIORCI SCREW
Smith & Nephew, Inc.
7207918
In Commercial Distribution

  • 03596010485540 ()
7207918

  • Bioabsorbable orthopaedic bone screw
TRESTLE LUXE II, ACP, 1-LEVEL, 20
ALPHATEC SPINE, INC.
711-0120
In Commercial Distribution

  • 00190376215129 ()

  • Height: 20 Millimeter


  • Spinal fixation plate, non-bioabsorbable
ECHELON POROUS 190MM STRAIGHT SZ 20
Smith & Nephew, Inc.
71340120
Not in Commercial Distribution

  • 03596010328793 ()
71340120

  • Coated hip femur prosthesis, modular
REFLECTION XLPE 28 20 +4 54-56
Smith & Nephew, Inc.
71339854
In Commercial Distribution

  • 03596010591814 ()
71339854

  • Non-constrained polyethylene acetabular liner
REFLECTION XLPE 32 20 +4 70-76
Smith & Nephew, Inc.
71339270
In Commercial Distribution

  • 03596010591807 ()
71339270

  • Non-constrained polyethylene acetabular liner
REFLECTION XLPE 32 20 +4 66-68
Smith & Nephew, Inc.
71339266
In Commercial Distribution

  • 03596010591791 ()
71339266

  • Non-constrained polyethylene acetabular liner
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