SEARCH RESULTS FOR: arthrex*(17702 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 UKA, SPACER BLOCK INSERT, 10MM
ARTHREX, INC.
AR-601-SB10
In Commercial Distribution

  • 00888867037366 ()
AR-601-SB10

  • Suturing unit, single-use
IBALANCE UKA, SPACER BLOCK INSERT, 9MM
ARTHREX, INC.
AR-601-SB09
In Commercial Distribution

  • 00888867037359 ()
AR-601-SB09

  • Suturing unit, single-use
IBALANCE UKA, SPACER BLOCK INSERT, 8MM
ARTHREX, INC.
AR-601-SB08
In Commercial Distribution

  • 00888867037342 ()
AR-601-SB08

  • Suturing unit, single-use
IBALANCE UKA, SPACER BLOCK INSERT, 7MM
ARTHREX, INC.
AR-601-SB07
In Commercial Distribution

  • 00888867037335 ()
AR-601-SB07

  • Suturing unit, single-use
IBALANCE UKA, SPACER BLOCK INSERT, 6MM
ARTHREX, INC.
AR-601-SB06
In Commercial Distribution

  • 00888867037328 ()
AR-601-SB06

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,10MM
ARTHREX, INC.
AR-601-PB10
In Commercial Distribution

  • 00888867037311 ()
AR-601-PB10

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,9MM
ARTHREX, INC.
AR-601-PB09
In Commercial Distribution

  • 00888867037304 ()
AR-601-PB09

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,8MM
ARTHREX, INC.
AR-601-PB08
In Commercial Distribution

  • 00888867037298 ()
AR-601-PB08

  • Suturing unit, single-use
IBAL UKA,POST RESCTION GD,7MM
ARTHREX, INC.
AR-601-PB07
In Commercial Distribution

  • 00888867037281 ()
AR-601-PB07

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,6MM
ARTHREX, INC.
AR-601-PB06
In Commercial Distribution

  • 00888867037274 ()
AR-601-PB06

  • Suturing unit, single-use
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