SEARCH RESULTS FOR: arthrex*(9019 results)

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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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iBALANCE TKA, LMR POST REF SIZER
ARTHREX, INC.
AR-605-4
In Commercial Distribution

  • 00888867038813 ()
AR-605-4

  • Suturing unit, single-use
iBALANCE TKA, LMR DISTAL CUT GUIDE
ARTHREX, INC.
AR-605-1
In Commercial Distribution

  • 00888867038769 ()
AR-605-1

  • Suturing unit, single-use
iBALANCE PFJ, ANTERIOR CUT GUIDE
ARTHREX, INC.
AR-602-9
In Commercial Distribution

  • 00888867038561 ()
AR-602-9

  • Surgical drill guide, reusable
IBAL PFJ,ANTERI CUT GD BASE,LFT
ARTHREX, INC.
AR-602-8L
In Commercial Distribution

  • 00888867038547 ()
AR-602-8L

  • Surgical drill guide, reusable
IBAL PFJ,PEGGED FEMTRL,SIZ 4,RT
ARTHREX, INC.
AR-602-57
In Commercial Distribution

  • 00888867038523 ()
AR-602-57

  • Suturing unit, single-use
IBAL PFJ,PEGGED FEMTRL,SIZ 2,RT
ARTHREX, INC.
AR-602-55
In Commercial Distribution

  • 00888867038509 ()
AR-602-55

  • Suturing unit, single-use
IBAL PFJ,PEGGED FEMTRL,SIZ 1,RT
ARTHREX, INC.
AR-602-54
In Commercial Distribution

  • 00888867038493 ()
AR-602-54

  • Suturing unit, single-use
IBAL PFJ,PEGGED FEM TRL,SIZ 4,LFT
ARTHREX, INC.
AR-602-53
In Commercial Distribution

  • 00888867038486 ()
AR-602-53

  • Suturing unit, single-use
IBAL PFJ,PEGGED FEM TRL,SIZ 2,LFT
ARTHREX, INC.
AR-602-51
In Commercial Distribution

  • 00888867038462 ()
AR-602-51

  • Suturing unit, single-use
IBAL PFJ,ANTERI CORTEX ALIGNMNT GD
ARTHREX, INC.
AR-602-5
In Commercial Distribution

  • 00888867038448 ()
AR-602-5

  • Surgical drill guide, reusable
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