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FDA 510(k), K090260, MODIFICATION TO:STRAUMANN GUIDED INSTRUMENTS
FDA 510(k), K090260, MODIFICATION TO:STRAUMANN GUIDED INSTRUMENTS
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510(K) Number: K090260
Device Name: MODIFICATION TO:STRAUMANN GUIDED INSTRUMENTS
Manufacturer: STRAUMANN MANUFACTURING, INC.
Device Classification Name: Implant, Endosseous, Root-Form
Regulation Number: 872.3640
Classification Product Code: DZE
Date Received: 02/03/2009
Decision Date: 02/26/2009
Regulation Medical Specialty: Dental
Device Name: MODIFICATION TO:STRAUMANN GUIDED INSTRUMENTS
Manufacturer: STRAUMANN MANUFACTURING, INC.
Device Classification Name: Implant, Endosseous, Root-Form
Regulation Number: 872.3640
Classification Product Code: DZE
Date Received: 02/03/2009
Decision Date: 02/26/2009
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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