SEARCH RESULTS FOR: 得克萨斯A(34825 results)

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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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Modular Trial, 20x17x8mm, 7 Deg Lordosis
Seaspine Orthopedics Corporation
SR-1105-08
In Commercial Distribution

  • 10889981318529 ()
SR-1105-08

  • Spinal implant trial
Modular Trial, 20x17x6mm, 7 Deg Lordosis
Seaspine Orthopedics Corporation
SR-1105-06
In Commercial Distribution

  • 10889981318512 ()
SR-1105-06

  • Spinal implant trial
Modular Trial, 20x17x5mm, 7 Deg Lordosis
Seaspine Orthopedics Corporation
SR-1105-05
In Commercial Distribution

  • 10889981318505 ()
SR-1105-05

  • Spinal implant trial
Modular Trial, 20x17x11mm, 7 Deg Lordosis
Seaspine Orthopedics Corporation
SR-1105-11
In Commercial Distribution

  • 10889981318499 ()
SR-1105-11

  • Spinal implant trial
Modular Trial, 20x17x7mm, 7 Deg Lordosis
Seaspine Orthopedics Corporation
SR-1105-07
In Commercial Distribution

  • 10889981318482 ()
SR-1105-07

  • Spinal implant trial
Cambria Trial 13 x 12 x 10mm, w/o Stop
Seaspine Orthopedics Corporation
SR-1085-10
In Commercial Distribution

  • 10889981310325 ()
SR-1085-10

  • Spinal implant trial
Cambria Trial 13 x 12 x 09mm, w/o Stop
Seaspine Orthopedics Corporation
SR-1085-09
In Commercial Distribution

  • 10889981310318 ()
SR-1085-09

  • Spinal implant trial
Cambria Trial 13 x 12 x 08mm, w/o Stop
Seaspine Orthopedics Corporation
SR-1085-08
In Commercial Distribution

  • 10889981310301 ()
SR-1085-08

  • Spinal implant trial
Cambria Trial 13 x 12 x 07mm, w/o Stop
Seaspine Orthopedics Corporation
SR-1085-07
In Commercial Distribution

  • 10889981310295 ()
SR-1085-07

  • Spinal implant trial
Cambria Trial 13 x 12 x 06mm, w/o Stop
Seaspine Orthopedics Corporation
SR-1085-06
In Commercial Distribution

  • 10889981310288 ()
SR-1085-06

  • Spinal implant trial
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