510(k) K182313
K182313 is an FDA 510(k) premarket notification submitted by Medical Instinct Deutschland GmbH for the device "BoneTrust Implant System". The FDA issued a decision of Substantially Equivalent on Mar 11, 2019. The device falls under product code DZE (Implant, Endosseous, Root-Form), a Class II device regulated under 21 CFR 872.3640. Medical Instinct Deutschland GmbH has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 11, 2019
- Date Received
- Aug 27, 2018
- Clearance Type
- Abbreviated
- 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)