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FDA 510(k), K010204, STRYKER NAVIGATION SYSTEM-KNEE MODULE
FDA 510(k), K010204, STRYKER NAVIGATION SYSTEM-KNEE MODULE
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$149.00 USD
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$149.00 USD
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510(K) Number: K010204
Device Name: STRYKER NAVIGATION SYSTEM-KNEE MODULE
Manufacturer: STRYKER CORP.
Device Classification Name: Neurological Stereotaxic Instrument
Regulation Number: 882.4560
Classification Product Code: HAW
Date Received: 01/23/2001
Decision Date: 08/31/2001
Regulation Medical Specialty: Neurology
Device Name: STRYKER NAVIGATION SYSTEM-KNEE MODULE
Manufacturer: STRYKER CORP.
Device Classification Name: Neurological Stereotaxic Instrument
Regulation Number: 882.4560
Classification Product Code: HAW
Date Received: 01/23/2001
Decision Date: 08/31/2001
Regulation Medical Specialty: Neurology
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