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FDA 510(k), K854749, STARTANIUS DENTAL IMPLANT SYSTEM
FDA 510(k), K854749, STARTANIUS DENTAL IMPLANT SYSTEM
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510(K) Number: K854749
Device Name: STARTANIUS DENTAL IMPLANT SYSTEM
Manufacturer: WIMMER
Device Classification Name: Implant, Endosseous, Root-Form
Regulation Number: DZE
Classification Product Code: 11/26/1985
Date Received: 03/06/1986
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: STARTANIUS DENTAL IMPLANT SYSTEM
Manufacturer: WIMMER
Device Classification Name: Implant, Endosseous, Root-Form
Regulation Number: DZE
Classification Product Code: 11/26/1985
Date Received: 03/06/1986
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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