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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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RING CURETTE,ANKLE ARTHRSCPY,STR
ARTHREX, INC.
AR-8655-14
In Commercial Distribution

  • 00888867044364 ()
AR-8655-14

  • Bone curette, reusable
DRILL GUIDE, ANKLE ARTHROSCOPY
ARTHREX, INC.
AR-8655-13
In Commercial Distribution

  • 00888867044357 ()
AR-8655-13

  • Surgical drill guide, reusable
ELEVATOR, ANKLE ARTHRO SCOPY, SHARP
ARTHREX, INC.
AR-8655-12
In Commercial Distribution

  • 00888867044340 ()
AR-8655-12

  • Bone lever/elevator, reusable
ELEVATOR, ANKLE ARTHROSCOPY, BLUNT
ARTHREX, INC.
AR-8655-11
In Commercial Distribution

  • 00888867044333 ()
AR-8655-11

  • Bone lever/elevator, reusable
COBB ELEVATOR, ANKLE ARTHROSCOPY
ARTHREX, INC.
AR-8655-10
In Commercial Distribution

  • 00888867044326 ()
AR-8655-10

  • Bone lever/elevator, reusable
OSTEOTOME, ANKLE ARTHRO SCOPY, CURVED
ARTHREX, INC.
AR-8655-09
In Commercial Distribution

  • 00888867044319 ()
AR-8655-09

  • Orthopaedic osteotome
OSTEOTOME, ANKLE ARTHRO SCOPY, STRAIGHT
ARTHREX, INC.
AR-8655-08
In Commercial Distribution

  • 00888867044302 ()
AR-8655-08

  • Orthopaedic osteotome
CHONDRAL PICK, ANKLE ARTHROSCOPY, 30 DEG
ARTHREX, INC.
AR-8655-05
In Commercial Distribution

  • 00888867044289 ()
AR-8655-05

  • Orthopaedic implant impactor, reusable
RING CURRETTE,ANKLE ARTHRSCPY,REVSE ANGL
ARTHREX, INC.
AR-8655-04
In Commercial Distribution

  • 00888867044272 ()
AR-8655-04

  • Bone curette, reusable
CUP CURRETTE,ANKLE ARTHRSCPY,SM ANGD
ARTHREX, INC.
AR-8655-03
In Commercial Distribution

  • 00888867044265 ()
AR-8655-03

  • Bone curette, reusable
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