SEARCH RESULTS FOR: arthrex*(8149 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 Class Implantable

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Arthrex® - 00888867037359

IBALANCE UKA, SPACER BLOCK INSERT, 9MM
ARTHREX, INC.
AR-601-SB09
In Commercial Distribution

  • 00888867037359 ()
AR-601-SB09

  • Suturing unit, single-use

Arthrex® - 00888867037342

IBALANCE UKA, SPACER BLOCK INSERT, 8MM
ARTHREX, INC.
AR-601-SB08
In Commercial Distribution

  • 00888867037342 ()
AR-601-SB08

  • Suturing unit, single-use

Arthrex® - 00888867037335

IBALANCE UKA, SPACER BLOCK INSERT, 7MM
ARTHREX, INC.
AR-601-SB07
In Commercial Distribution

  • 00888867037335 ()
AR-601-SB07

  • Suturing unit, single-use

Arthrex® - 00888867037328

IBALANCE UKA, SPACER BLOCK INSERT, 6MM
ARTHREX, INC.
AR-601-SB06
In Commercial Distribution

  • 00888867037328 ()
AR-601-SB06

  • Suturing unit, single-use

Arthrex® - 00888867037311

IBAL UKA,POST RESECT GD,10MM
ARTHREX, INC.
AR-601-PB10
In Commercial Distribution

  • 00888867037311 ()
AR-601-PB10

  • Suturing unit, single-use

Arthrex® - 00888867037304

IBAL UKA,POST RESECT GD,9MM
ARTHREX, INC.
AR-601-PB09
In Commercial Distribution

  • 00888867037304 ()
AR-601-PB09

  • Suturing unit, single-use

Arthrex® - 00888867037298

IBAL UKA,POST RESECT GD,8MM
ARTHREX, INC.
AR-601-PB08
In Commercial Distribution

  • 00888867037298 ()
AR-601-PB08

  • Suturing unit, single-use

Arthrex® - 00888867037281

IBAL UKA,POST RESCTION GD,7MM
ARTHREX, INC.
AR-601-PB07
In Commercial Distribution

  • 00888867037281 ()
AR-601-PB07

  • Suturing unit, single-use

Arthrex® - 00888867037274

IBAL UKA,POST RESECT GD,6MM
ARTHREX, INC.
AR-601-PB06
In Commercial Distribution

  • 00888867037274 ()
AR-601-PB06

  • Suturing unit, single-use

Arthrex® - 00888867037267

IBAL UKA,POST RESECT GD,5MM
ARTHREX, INC.
AR-601-PB05
In Commercial Distribution

  • 00888867037267 ()
AR-601-PB05

  • Suturing unit, single-use
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