510(k) K201700
K201700 is an FDA 510(k) premarket notification submitted by Bego Implant Systems GmbH & Co. KG for the device "BEGO Semados® RS/RSX Implant System". The FDA issued a decision of Substantially Equivalent on Jan 13, 2021. The device falls under product code DZE (Implant, Endosseous, Root-Form), a Class II device regulated under 21 CFR 872.3640. Bego Implant Systems GmbH & Co. KG has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 13, 2021
- Date Received
- Jun 22, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Implant, Endosseous, Root-Form
- Device Class
- Class II
- Regulation Number
- 872.3640
- Review Panel
- DE
- Submission Type
- 510(k)