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FDA 510(k), K200265, Surgical Drills
FDA 510(k), K200265, Surgical Drills
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$149.00 USD
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$149.00 USD
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510(K) Number: K200265
Device Name: Surgical Drills
Manufacturer: Implant Direct Sybron Manufacturing, LLC
Device Classification Name: Drill, Bone, Powered
Regulation Number: 872.4120
Classification Product Code: DZI
Date Received: 02/03/2020
Decision Date: 06/30/2020
Regulation Medical Specialty: Dental
Device Name: Surgical Drills
Manufacturer: Implant Direct Sybron Manufacturing, LLC
Device Classification Name: Drill, Bone, Powered
Regulation Number: 872.4120
Classification Product Code: DZI
Date Received: 02/03/2020
Decision Date: 06/30/2020
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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