SEARCH RESULTS FOR: Femoral(172121 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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SL-PLUS STEM LATERAL NON-CEMENTED 10
Smith & Nephew, Inc.
75002768
In Commercial Distribution

  • 07611996078107 ()
75002768

  • Press-fit femoral stem prosthesis
SL-PLUS STEM LATERAL NON-CEMENTED 9
Smith & Nephew, Inc.
75002766
In Commercial Distribution

  • 07611996078091 ()
75002766

  • Press-fit femoral stem prosthesis
SL-PLUS STEM LATERAL NON-CEMENTED 8
Smith & Nephew, Inc.
75002764
In Commercial Distribution

  • 07611996078084 ()
75002764

  • Press-fit femoral stem prosthesis
SL-PLUS STEM LATERAL NON-CEMENTED 6
Smith & Nephew, Inc.
75002760
In Commercial Distribution

  • 07611996078060 ()
75002760

  • Press-fit femoral stem prosthesis
SL-PLUS STEM LATERAL NON-CEMENTED 5
Smith & Nephew, Inc.
75002758
In Commercial Distribution

  • 07611996078053 ()
75002758

  • Press-fit femoral stem prosthesis
SL-PLUS STEM LATERAL NON-CEMENTED 4
Smith & Nephew, Inc.
75002756
In Commercial Distribution

  • 07611996078046 ()
75002756

  • Press-fit femoral stem prosthesis
SL-PLUS STEM LATERAL NON-CEMENTED 2
Smith & Nephew, Inc.
75002750
In Commercial Distribution

  • 07611996078022 ()
75002750

  • Press-fit femoral stem prosthesis
SLR-PLUS REVISION STEM LATERAL 9 NON-CEM
Smith & Nephew, Inc.
75001934
In Commercial Distribution

  • 07611996088335 ()
75001934

  • Press-fit femoral stem prosthesis
SLR-PLUS REVISION STEM LATERAL 8 NON-CEM
Smith & Nephew, Inc.
75001933
In Commercial Distribution

  • 07611996088328 ()
75001933

  • Press-fit femoral stem prosthesis
SLR-PLUS REVISION STEM LATERAL 7 NON-CEM
Smith & Nephew, Inc.
75001932
In Commercial Distribution

  • 07611996088311 ()
75001932

  • Press-fit femoral stem prosthesis
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