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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K-Wire, Blunt, Nitinol, 680
SEASPINE ORTHOPEDICS CORPORATION
28-40-0018-680
In Commercial Distribution

  • 10889981116781 ()

  • 680
28-40-0018-680

  • Catheter stylet
K-Wire, Blunt, Nitinol, 500
SEASPINE ORTHOPEDICS CORPORATION
28-40-0018-500
In Commercial Distribution

  • 10889981116774 ()

  • 500
28-40-0018-500

  • Catheter stylet
K-Wire, Blunt, Nitinol, 380
SEASPINE ORTHOPEDICS CORPORATION
28-40-0018-380
In Commercial Distribution

  • 10889981116767 ()

  • 380
28-40-0018-380

  • Catheter stylet
K-Wire, Bevel, Nitinol, 680
SEASPINE ORTHOPEDICS CORPORATION
28-40-0017-680
In Commercial Distribution

  • 10889981116750 ()

  • 680
28-40-0017-680

  • Catheter stylet
K-Wire, Bevel, Nitinol, 500
SEASPINE ORTHOPEDICS CORPORATION
28-40-0017-500
In Commercial Distribution

  • 10889981116743 ()

  • 500
28-40-0017-500

  • Catheter stylet
K-Wire, Bevel, Nitinol, 380
SEASPINE ORTHOPEDICS CORPORATION
28-40-0017-380
In Commercial Distribution

  • 10889981116736 ()

  • 380
28-40-0017-380

  • Catheter stylet
K-Wire, Blunt, SS, 680
SEASPINE ORTHOPEDICS CORPORATION
28-40-0016-680
In Commercial Distribution

  • 10889981116729 ()

  • 680
28-40-0016-680

  • Catheter stylet
K-Wire, Blunt, SS, 500
SEASPINE ORTHOPEDICS CORPORATION
28-40-0016-500
In Commercial Distribution

  • 10889981116712 ()

  • 500
28-40-0016-500

  • Catheter stylet
K-Wire, Blunt, SS, 380
SEASPINE ORTHOPEDICS CORPORATION
28-40-0016-380
In Commercial Distribution

  • 10889981116705 ()

  • 380
28-40-0016-380

  • Catheter stylet
K-Wire, Bevel, SS, 680
SEASPINE ORTHOPEDICS CORPORATION
28-40-0015-680
In Commercial Distribution

  • 10889981116699 ()

  • 680
28-40-0015-680

  • Catheter stylet
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