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 Type Device Class Implantable

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Fixed Trial; 32x14 (05-3524)
SEASPINE ORTHOPEDICS CORPORATION
29-20-3214
In Commercial Distribution

  • 10889981041359 ()

  • 32mm x 14mm
29-20-3214

  • Spinal implant trial
Fixed Trial; 32x13 (05-3523)
SEASPINE ORTHOPEDICS CORPORATION
29-20-3213
In Commercial Distribution

  • 10889981041342 ()

  • 32mm x 13mm
29-20-3213

  • Spinal implant trial
Fixed Trial; 32x12 (05-3522)
SEASPINE ORTHOPEDICS CORPORATION
29-20-3212
In Commercial Distribution

  • 10889981041335 ()

  • 32mm x 12mm
29-20-3212

  • Spinal implant trial
Fixed Trial; 32x10 (05-3520)
SEASPINE ORTHOPEDICS CORPORATION
29-20-3210
In Commercial Distribution

  • 10889981041311 ()

  • 32mm x 10mm
29-20-3210

  • Spinal implant trial
Fixed Trial; 32x8 (05-3528)
SEASPINE ORTHOPEDICS CORPORATION
29-20-3208
In Commercial Distribution

  • 10889981041298 ()

  • 32mm x 8mm
29-20-3208

  • Spinal implant trial
Fixed Trial; 27x12 (05-3512)
SEASPINE ORTHOPEDICS CORPORATION
29-20-2712
In Commercial Distribution

  • 10889981041250 ()

  • 27mm x 12mm
29-20-2712

  • Spinal implant trial
Fixed Trial; 27x10 (05-3510)
SEASPINE ORTHOPEDICS CORPORATION
29-20-2710
In Commercial Distribution

  • 10889981041236 ()

  • 27mm x 10mm
29-20-2710

  • Spinal implant trial
Fixed Trial; 27x9 (05-3519)
SEASPINE ORTHOPEDICS CORPORATION
29-20-2709
In Commercial Distribution

  • 10889981041229 ()

  • 27mm x 9mm
29-20-2709

  • Spinal implant trial
10mm x 28mm x 12mm, 6-20 Deg
SEASPINE ORTHOPEDICS CORPORATION
83-2820
In Commercial Distribution

  • 10889981140038 ()

  • 10mm x 28mm x 12mm, 6-20 Deg
83-2820

  • Polymeric spinal interbody fusion cage
10mm x 28mm x 10mm, 3-17 Deg
SEASPINE ORTHOPEDICS CORPORATION
83-2817
In Commercial Distribution

  • 10889981140021 ()

  • 10mm x 28mm x 10mm, 3-17 Deg
83-2817

  • Polymeric spinal interbody fusion cage
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