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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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TC-PLUS PRIMARY / TC-PLUS REVISION TIBIAL INSERT TC PS 8/9
Smith & Nephew, Inc.
75005197
In Commercial Distribution

  • 07611996073720 ()
75005197

  • Tibial insert
TC PRIM/TC REV TIB INSERT TC PS 6/21
Smith & Nephew, Inc.
75005195
In Commercial Distribution

  • 07611996073706 ()
75005195

  • Tibial insert
TC-PLUS PRIMARY / TC-PLUS REVISION TIBIAL INSERT TC PS 6/19
Smith & Nephew, Inc.
75005194
In Commercial Distribution

  • 07611996073690 ()
75005194

  • Tibial insert
TC PRIM/TC REV TIB INSERT TC PS 6/17
Smith & Nephew, Inc.
75005193
In Commercial Distribution

  • 07611996073683 ()
75005193

  • Tibial insert
TC-PLUS PRIMARY / TC-PLUS REVISION TIBIAL INSERT TC PS 6/15
Smith & Nephew, Inc.
75005192
In Commercial Distribution

  • 07611996073676 ()
75005192

  • Tibial insert
TC-PLUS PRIMARY / TC-PLUS REVISION TIBIAL INSERT TC PS 6/13
Smith & Nephew, Inc.
75005191
In Commercial Distribution

  • 07611996073669 ()
75005191

  • Tibial insert
TC-PLUS PRIMARY / TC-PLUS REVISION TIBIAL INSERT TC PS 6/11
Smith & Nephew, Inc.
75005190
In Commercial Distribution

  • 07611996073652 ()
75005190

  • Tibial insert
TC-PLUS PRIMARY / TC-PLUS REVISION TIBIAL INSERT TC PS 6/9
Smith & Nephew, Inc.
75005189
In Commercial Distribution

  • 07611996073645 ()
75005189

  • Tibial insert
TC PRIM/TC REV TIB INSERT TC PS 4/21
Smith & Nephew, Inc.
75005187
In Commercial Distribution

  • 07611996073621 ()
75005187

  • Tibial insert
TC-PLUS PRIMARY / TC-PLUS REVISION TIBIAL INSERT TC PS 4/19
Smith & Nephew, Inc.
75005186
In Commercial Distribution

  • 07611996073614 ()
75005186

  • Tibial insert
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