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

Show Filters

Filters are currently being applied
31x24mm 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
21-20-3110
In Commercial Distribution

  • 10889981037949 ()

  • 31x24mm 10mm 8°
21-20-3110

  • Spinal implant trial
31x24mm 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
21-20-3108
In Commercial Distribution

  • 10889981037932 ()

  • 31x24mm 8mm 8°
21-20-3108

  • 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 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
Trial, 32mm x 25mm x 22mm, 8 Deg. Zuma™ Trials are used to determine the appropriate Zuma implant size.
SEASPINE ORTHOPEDICS CORPORATION
95-5222
In Commercial Distribution

  • 10889981037697 ()

  • 32mm x 25mm x 22mm, 8°
95-5222

  • Spinal implant trial
Trial, 32mm x 25mm x 20mm, 8 Deg. Zuma™ Trials are used to determine the appropriate Zuma implant size.
SEASPINE ORTHOPEDICS CORPORATION
95-5220
In Commercial Distribution

  • 10889981037680 ()

  • 32mm x 25mm x 20mm, 8°
95-5220

  • Spinal implant trial
Trial, 32mm x 25mm x 18mm, 8 Deg. Zuma™ Trials are used to determine the appropriate Zuma implant size.
SEASPINE ORTHOPEDICS CORPORATION
95-5218
In Commercial Distribution

  • 10889981037673 ()

  • 32mm x 25mm x 18mm, 8°
95-5218

  • Spinal implant trial
< 1 ... 130 131 132 133 134 ... 202 >