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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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INSTRUMENT 9560609 BAYON 5MM 90
MEDTRONIC SOFAMOR DANEK, INC.
9560609
In Commercial Distribution

  • 00673978960722 ()


  • Bone curette, reusable
INSTRUMENT 9560608 BAYON 5MM 40
MEDTRONIC SOFAMOR DANEK, INC.
9560608
In Commercial Distribution

  • 00673978960715 ()


  • Bone curette, reusable
INSTRUMENT 9560607 BAYON 4MM 90
MEDTRONIC SOFAMOR DANEK, INC.
9560607
In Commercial Distribution

  • 00673978960708 ()


  • Bone curette, reusable
INSTRUMENT 9560606 BAYON 4MM 40
MEDTRONIC SOFAMOR DANEK, INC.
9560606
In Commercial Distribution

  • 00673978960692 ()


  • Bone curette, reusable
INSTRUMENT 9560605 BAYON 3MM 90
MEDTRONIC SOFAMOR DANEK, INC.
9560605
In Commercial Distribution

  • 00673978960685 ()


  • Bone curette, reusable
INSTRUMENT 9560604 BAYON KERRISON 3MM 40
MEDTRONIC SOFAMOR DANEK, INC.
9560604
In Commercial Distribution

  • 00673978960678 ()


  • Bone curette, reusable
INSTRUMENT 9560603 BAYONTD KRNSON 2MM 90
MEDTRONIC SOFAMOR DANEK, INC.
9560603
In Commercial Distribution

  • 00673978960661 ()


  • Bone curette, reusable
INSTRUMENT 9560602 BAYON 2MM 40
MEDTRONIC SOFAMOR DANEK, INC.
9560602
In Commercial Distribution

  • 00673978960654 ()


  • Bone curette, reusable
INSTRUMENT 9560601 BAYON 1MM 90
MEDTRONIC SOFAMOR DANEK, INC.
9560601
In Commercial Distribution

  • 00673978960647 ()


  • Bone curette, reusable
INSTRUMENT 9560600 BAYON 1MM 40
MEDTRONIC SOFAMOR DANEK, INC.
9560600
In Commercial Distribution

  • 00673978960630 ()


  • Bone curette, reusable
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