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 Class Implantable

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Trial Rasp, 43mm x 30mm x 12mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-241210
In Commercial Distribution

  • 10889981310035 ()
RA2-241210

  • Bone file/rasp, manual, reusable
Trial Rasp, 43mm x 30mm x 10mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-241010
In Commercial Distribution

  • 10889981310028 ()
RA2-241010

  • Bone file/rasp, manual, reusable
Trial Rasp, 39mm x 30mm x 20mm, 25 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-232025
In Commercial Distribution

  • 10889981310011 ()
RA2-232025

  • Bone file/rasp, manual, reusable
Trial Rasp, 39mm x 30mm x 18mm, 25 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-231825
In Commercial Distribution

  • 10889981310004 ()
RA2-231825

  • Bone file/rasp, manual, reusable
Trial Rasp, 39mm x 30mm x 18mm, 20 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-231820
In Commercial Distribution

  • 10889981309992 ()
RA2-231820

  • Bone file/rasp, manual, reusable
Trial Rasp, 39mm x 30mm x 16mm, 20 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-231620
In Commercial Distribution

  • 10889981309985 ()
RA2-231620

  • Bone file/rasp, manual, reusable
Trial Rasp, 39mm x 30mm x 16mm, 15 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-231615
In Commercial Distribution

  • 10889981309978 ()
RA2-231615

  • Bone file/rasp, manual, reusable
Trial Rasp, 39mm x 30mm x 16mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-231610
In Commercial Distribution

  • 10889981309961 ()
RA2-231610

  • Bone file/rasp, manual, reusable
Trial Rasp, 39mm x 30mm x 14mm, 20 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-231420
In Commercial Distribution

  • 10889981309954 ()
RA2-231420

  • Bone file/rasp, manual, reusable
Trial Rasp, 39mm x 30mm x 14mm, 15 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-231415
In Commercial Distribution

  • 10889981309947 ()
RA2-231415

  • Bone file/rasp, manual, reusable
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