FDA 510(k), K961382, MT1A

FDA 510(k), K961382, MT1A

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510(K) Number: K961382
Device Name: MT1A
Manufacturer: THE EMERGING TECHNOLOGIES GROUP
Device Classification Name: implant, endosseous, root-form
Regulation Number: 872.3640
Classification Product Code: DZE
Date Received: 03/19/1996
Decision Date: 09/25/1996
Regulation Medical Specialty: Dental

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