SEARCH RESULTS FOR: arthrex*(9631 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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3.8x130MM FIBULA NAIL, LEFT
ARTHREX, INC.
AR-8973L-38-130
In Commercial Distribution

  • 00888867295247 ()
AR-8973L-38-130

  • Arthrodesis intramedullary nail, non-distracting
3.0X180MM FIBULA NAIL, RIGHT
ARTHREX, INC.
AR-8973R-30-180
In Commercial Distribution

  • 00888867295230 ()
AR-8973R-30-180

  • Arthrodesis intramedullary nail, non-distracting
3.0X180MM FIBULA NAIL, LEFT
ARTHREX, INC.
AR-8973L-30-180
In Commercial Distribution

  • 00888867295223 ()
AR-8973L-30-180

  • Arthrodesis intramedullary nail, non-distracting
3.0X130MM FIBULA NAIL, RIGHT
ARTHREX, INC.
AR-8973R-30-130
In Commercial Distribution

  • 00888867295216 ()
AR-8973R-30-130

  • Arthrodesis intramedullary nail, non-distracting
3.0X130MM FIBULA NAIL, LEFT
ARTHREX, INC.
AR-8973L-30-130
In Commercial Distribution

  • 00888867295209 ()
AR-8973L-30-130

  • Arthrodesis intramedullary nail, non-distracting
Ø12 X 30MM PEEK IF SCRW NON-VENTED
ARTHREX, INC.
AR-4030P-12
In Commercial Distribution

  • 00888867295094 ()
AR-4030P-12

  • Tendon/ligament bone anchor, non-bioabsorbable
Ø11 X 30MM PEEK IF SCRW NON-VENTED
ARTHREX, INC.
AR-4030P-11
In Commercial Distribution

  • 00888867295087 ()
AR-4030P-11

  • Tendon/ligament bone anchor, non-bioabsorbable
Ø10 X 30MM PEEK IF SCRW NON-VENTED
ARTHREX, INC.
AR-4030P-10
In Commercial Distribution

  • 00888867295070 ()
AR-4030P-10

  • Tendon/ligament bone anchor, non-bioabsorbable
Ø9 X 30MM PEEK IF SCRW NON-VENTED
ARTHREX, INC.
AR-4030P-09
In Commercial Distribution

  • 00888867295063 ()
AR-4030P-09

  • Tendon/ligament bone anchor, non-bioabsorbable
Ø8 X 30MM PEEK IF SCRW NON-VENTED
ARTHREX, INC.
AR-4030P-08
In Commercial Distribution

  • 00888867295056 ()
AR-4030P-08

  • Tendon/ligament bone anchor, non-bioabsorbable
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