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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 Type Device Class Implantable

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27x21mm Trial 14mm 8 deg. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-20-2714
In Commercial Distribution

  • 10889981037918 ()

  • 27x21mm 14mm 8°
21-20-2714

  • Spinal implant trial
27x21mm Trial 12mm 8 deg. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-20-2712
In Commercial Distribution

  • 10889981037901 ()

  • 27x21mm 12mm 8°
21-20-2712

  • Spinal implant trial
27x21mm Trial 10mm 8 deg. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-20-2710
In Commercial Distribution

  • 10889981037895 ()

  • 27x21mm 10mm 8°
21-20-2710

  • Spinal implant trial
27x21mm Trial 8mm 8 deg. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-20-2708
In Commercial Distribution

  • 10889981037888 ()

  • 27x21mm 8mm 8°
21-20-2708

  • Spinal implant trial
39x30 16mm Spin Plate. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-11-3916
In Commercial Distribution

  • 10889981037871 ()

  • 39x30 16mm
21-11-3916

  • Bone-screw internal spinal fixation system, non-sterile
39x30 14mm Spin Plate. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-11-3914
In Commercial Distribution

  • 10889981037864 ()

  • 39x30 14mm
21-11-3914

  • Bone-screw internal spinal fixation system, non-sterile
39x30 12mm Spin Plate. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-11-3912
In Commercial Distribution

  • 10889981037857 ()

  • 39x30 12mm
21-11-3912

  • Bone-screw internal spinal fixation system, non-sterile
39x30 10mm Spin Plate. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-11-3910
In Commercial Distribution

  • 10889981037840 ()

  • 39x30 10mm
21-11-3910

  • Bone-screw internal spinal fixation system, non-sterile
39x30 8mm Spin Plate. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-11-3908
In Commercial Distribution

  • 10889981037833 ()

  • 39x30 8mm
21-11-3908

  • Bone-screw internal spinal fixation system, non-sterile
35x27 16mm Spin Plate. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-11-3516
In Commercial Distribution

  • 10889981037826 ()

  • 35x27 16mm
21-11-3516

  • Bone-screw internal spinal fixation system, non-sterile
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