6 results
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50ms
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Sources: EU EUDAMED, US FDA
DREVE AMERICA CORP.
FDA registration
DREVE AMERICA CORP.·3 products·🇺🇸 United States
SCORPIO PS TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall component fit, ligament stability, and joint range of motion prior to final implantation of the insert to the tray.
FDA Recall
Terminated
·Stryker Howmedica Osteonics Corp.·Product code LXH·July 13, 2010
SCORPIO CR TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall component fit, ligament stability, and joint range of motion prior to final implantation of the insert to the tray.
FDA Recall
Terminated
·Stryker Howmedica Osteonics Corp.·Product code JWH·July 13, 2010
SCORPIO-FLEX PS TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall component fit, ligament stability, and joint range of motion prior to final implantation of the insert to the tray.
FDA Recall
Terminated
·Stryker Howmedica Osteonics Corp.·Product code LXH·July 13, 2010
SCORPIO-FLEX CR TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall component fit, ligament stability, and joint range of motion prior to final implantation of the insert to the tray.
FDA Recall
Terminated
·Stryker Howmedica Osteonics Corp.·Product code LXH·July 13, 2010
Advena Limited
Authorized representative
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