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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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TriMax Posterior 4 in 1 Pegged Cut Guide Open Size 6
Ortho Development Corporation
265-1056
In Commercial Distribution

  • 00822409108404 ()


  • Osteotomy guide, reusable
TriMax Posterior 4 in 1 Pegged Cut Guide Open Size 5
Ortho Development Corporation
265-1055
In Commercial Distribution

  • 00822409108398 ()


  • Osteotomy guide, reusable
TriMax Posterior 4 in 1 Pegged Cut Guide Open Size 4
Ortho Development Corporation
265-1054
In Commercial Distribution

  • 00822409108381 ()


  • Osteotomy guide, reusable
TriMax Posterior 4 in 1 Pegged Cut Guide Open Size 3
Ortho Development Corporation
265-1053
In Commercial Distribution

  • 00822409108374 ()


  • Osteotomy guide, reusable
TriMax Posterior 4 in 1 Pegged Cut Guide Open Size 2
Ortho Development Corporation
265-1052
In Commercial Distribution

  • 00822409108367 ()


  • Osteotomy guide, reusable
TriMax Posterior 4 in 1 Pegged Cut Guide Open Size 1
Ortho Development Corporation
265-1051
In Commercial Distribution

  • 00822409108350 ()


  • Osteotomy guide, reusable
Posterior 4 in 1 A/P Cut Guide Closed Size 7
Ortho Development Corporation
261-1017
In Commercial Distribution

  • 00822409048915 ()


  • Osteotomy guide, reusable
Posterior 4 in 1 A/P Cut Guide Closed Size 6
Ortho Development Corporation
261-1016
In Commercial Distribution

  • 00822409048908 ()


  • Osteotomy guide, reusable
Posterior 4 in 1 A/P Cut Guide Closed Size 5
Ortho Development Corporation
261-1015
In Commercial Distribution

  • 00822409048892 ()


  • Osteotomy guide, reusable
Posterior 4 in 1 A/P Cut Guide Closed Size 4
Ortho Development Corporation
261-1014
In Commercial Distribution

  • 00822409048885 ()


  • Osteotomy guide, reusable
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