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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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39x30mm Trial 16mm 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
21-20-3916
In Commercial Distribution

  • 10889981038076 ()

  • 39x30mm 16mm 8°
21-20-3916

  • Spinal implant trial
39x30mm 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
21-20-3912
In Commercial Distribution

  • 10889981038052 ()

  • 39x30mm 12mm 8°
21-20-3912

  • Spinal implant trial
39x30mm 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
21-20-3910
In Commercial Distribution

  • 10889981038045 ()

  • 39x30mm 10mm 8°
21-20-3910

  • Spinal implant trial
35x27mm Trial 16mm 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
21-20-3516
In Commercial Distribution

  • 10889981038021 ()

  • 35x27mm 16mm 8°
21-20-3516

  • Spinal implant trial
35x27mm 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
21-20-3512
In Commercial Distribution

  • 10889981038007 ()

  • 35x27mm 12mm 8°
21-20-3512

  • Spinal implant trial
35x27mm 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
21-20-3510
In Commercial Distribution

  • 10889981037994 ()

  • 35x27mm 10mm 8°
21-20-3510

  • Spinal implant trial
31x24mm Trial 16mm 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
21-20-3116
In Commercial Distribution

  • 10889981037970 ()

  • 31x24mm 16mm 8°
21-20-3116

  • Spinal implant trial
31x24mm 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
21-20-3112
In Commercial Distribution

  • 10889981037956 ()

  • 31x24mm 12mm 8°
21-20-3112

  • Spinal implant trial
27x21mm Trial 16mm 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
21-20-2716
In Commercial Distribution

  • 10889981037925 ()

  • 27x21mm 16mm 8°
21-20-2716

  • 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
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