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FDA 510(k), K073116, EBI INTERNAL IMPLANT SYSTEM
FDA 510(k), K073116, EBI INTERNAL IMPLANT SYSTEM
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510(K) Number: K073116
Device Name: EBI INTERNAL IMPLANT SYSTEM
Manufacturer: EBI, INC.
Device Classification Name: implant, endosseous, root-form
Regulation Number: 872.3640
Classification Product Code: DZE
Date Received: 11/05/2007
Decision Date: 02/28/2008
Regulation Medical Specialty: Dental
Device Name: EBI INTERNAL IMPLANT SYSTEM
Manufacturer: EBI, INC.
Device Classification Name: implant, endosseous, root-form
Regulation Number: 872.3640
Classification Product Code: DZE
Date Received: 11/05/2007
Decision Date: 02/28/2008
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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