FDA 510(k), K052871, STRYKER CUSTOM TI IMPLANT

FDA 510(k), K052871, STRYKER CUSTOM TI IMPLANT

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510(K) Number: K052871
Device Name: STRYKER CUSTOM TI IMPLANT
Manufacturer: STRYKER LEIBINGER
Device Classification Name: plate, cranioplasty, preformed, non-alterable
Regulation Number: 882.5330
Classification Product Code: GXN
Date Received: 10/11/2005
Decision Date: 12/16/2005
Regulation Medical Specialty: Neurology

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