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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
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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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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