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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 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 Pegged Cut Guide Closed Size 7
Ortho Development Corporation
261-1067
In Commercial Distribution

  • 00822409108343 ()


  • Osteotomy guide, reusable
Posterior 4 in 1 A/P Pegged Cut Guide Closed Size 6
Ortho Development Corporation
261-1066
In Commercial Distribution

  • 00822409108336 ()


  • Osteotomy guide, reusable
Posterior 4 in 1 A/P Pegged Cut Guide Closed Size 5
Ortho Development Corporation
261-1065
In Commercial Distribution

  • 00822409108329 ()


  • Osteotomy guide, reusable
Posterior 4 in 1 A/P Pegged Cut Guide Closed Size 4
Ortho Development Corporation
261-1064
In Commercial Distribution

  • 00822409108312 ()


  • Osteotomy guide, reusable
Posterior 4 in 1 A/P Pegged Cut Guide Closed Size 3
Ortho Development Corporation
261-1063
In Commercial Distribution

  • 00822409108305 ()


  • Osteotomy guide, reusable
Posterior 4 in 1 A/P Pegged Cut Guide Closed Size 2
Ortho Development Corporation
261-1062
In Commercial Distribution

  • 00822409108299 ()


  • Osteotomy guide, reusable
Posterior 4 in 1 A/P Pegged Cut Guide Closed Size 1
Ortho Development Corporation
261-1061
In Commercial Distribution

  • 00822409108282 ()


  • Osteotomy guide, reusable
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