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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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iTotal® Posterior Stabilized (PS) Knee Insert Kit
Conformis, Inc.
RPS010100002
In Commercial Distribution

  • M572RPS0101000021 ()

  • 10mm thick on the medial side, lateral side is patient specific
RPS0101000

  • Total knee prosthesis implantation guide-instrument kit
  • Tibial insert
N/A
Conformis, Inc.
RPS010100001
In Commercial Distribution

  • M572RPS0101000011 ()

  • 10mm thick on the medial side, lateral side is patient specific
RPS0101000

  • Total knee prosthesis implantation guide-instrument kit
  • Tibial insert
iTotal® Posterior Stabilized (PS) Knee Insert Kit
Conformis, Inc.
RPS010090002
In Commercial Distribution

  • M572RPS0100900021 ()

  • 9mm thick on the medial side, lateral side is patient specific
RPS0100900

  • Total knee prosthesis implantation guide-instrument kit
  • Tibial insert
N/A
Conformis, Inc.
RPS010090001
In Commercial Distribution

  • M572RPS0100900011 ()

  • 9mm thick on the medial side, lateral side is patient specific
RPS0100900

  • Total knee prosthesis implantation guide-instrument kit
  • Tibial insert
iTotal® Posterior Stabilized (PS) Knee Insert Kit
Conformis, Inc.
RPS010080002
In Commercial Distribution

  • M572RPS0100800021 ()

  • 8mm thick on the medial side, lateral side is patient specific
RPS0100800

  • Total knee prosthesis implantation guide-instrument kit
  • Tibial insert
N/A
Conformis, Inc.
RPS010080001
In Commercial Distribution

  • M572RPS0100800011 ()

  • 8mm thick on the medial side, lateral side is patient specific
RPS0100800

  • Total knee prosthesis implantation guide-instrument kit
  • Tibial insert
iTotal® Posterior Stabilized (PS) Knee Insert Kit
Conformis, Inc.
RPS010070002
In Commercial Distribution

  • M572RPS0100700021 ()

  • 7mm thick on the medial side, lateral side is patient specific
RPS0100700

  • Total knee prosthesis implantation guide-instrument kit
  • Tibial insert
N/A
Conformis, Inc.
RPS010070001
In Commercial Distribution

  • M572RPS0100700011 ()

  • 7mm thick on the medial side, lateral side is patient specific
RPS0100700

  • Total knee prosthesis implantation guide-instrument kit
  • Tibial insert
iTotal® Posterior Stabilized (PS) Knee Insert Kit
Conformis, Inc.
RPS010060002
In Commercial Distribution

  • M572RPS0100600021 ()

  • 6mm thick on the medial side, lateral side is patient specific
RPS0100600

  • Total knee prosthesis implantation guide-instrument kit
  • Tibial insert
The standard rearfoot screw is used in the Integra Total Foot System. It is made from titanium and is non-locking.
Ascension Orthopedics, Inc.
2845145
In Commercial Distribution

  • 10381780118671 ()
  • M26828451451 ()

  • 45 mm L x 3.5 mm dia
2845145

  • Orthopaedic bone screw, non-bioabsorbable, non-sterile
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