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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8mm Hollywood Trial, Lordotic
SEASPINE ORTHOPEDICS CORPORATION
93-4251
In Commercial Distribution

  • 10889981031206 ()

  • 8mm
93-4251

  • Spinal implant trial
7mm Hollywood Trial, Lordotic
SEASPINE ORTHOPEDICS CORPORATION
93-4250
In Commercial Distribution

  • 10889981031190 ()

  • 7mm
93-4250

  • Spinal implant trial
18mm Hollywood Trial, Lordotic, Short
SEASPINE ORTHOPEDICS CORPORATION
93-4242
In Commercial Distribution

  • 10889981031183 ()

  • 18mm
93-4242

  • Spinal implant trial
17mm Hollywood Trial, Lordotic, Short
SEASPINE ORTHOPEDICS CORPORATION
93-4241
In Commercial Distribution

  • 10889981031176 ()

  • 17mm
93-4241

  • Spinal implant trial
16mm Hollywood Trial, Lordotic, Short
SEASPINE ORTHOPEDICS CORPORATION
93-4240
In Commercial Distribution

  • 10889981031169 ()

  • 16mm
93-4240

  • Spinal implant trial
14mm Hollywood Trial, Lordotic, Short
SEASPINE ORTHOPEDICS CORPORATION
93-4238
In Commercial Distribution

  • 10889981031145 ()

  • 14mm
93-4238

  • Spinal implant trial
12mm Hollywood Trial, Lordotic, Short
SEASPINE ORTHOPEDICS CORPORATION
93-4236
In Commercial Distribution

  • 10889981031121 ()

  • 12mm
93-4236

  • Spinal implant trial
9mm Hollywood Trial, Lordotic, Short
SEASPINE ORTHOPEDICS CORPORATION
93-4233
In Commercial Distribution

  • 10889981031091 ()

  • 9mm
93-4233

  • Spinal implant trial
8mm Hollywood Trial, Lordotic, Short
SEASPINE ORTHOPEDICS CORPORATION
93-4232
In Commercial Distribution

  • 10889981031084 ()

  • 8mm
93-4232

  • Spinal implant trial
7mm Hollywood Trial, Lordotic, Short
SEASPINE ORTHOPEDICS CORPORATION
93-4231
In Commercial Distribution

  • 10889981031077 ()

  • 7mm
93-4231

  • Spinal implant trial
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