510(k) K230797
K230797 is an FDA 510(k) premarket notification submitted by Sprig Oral Health Technologies, Inc. for the device "SmartMTA Capsule". The FDA issued a decision of Substantially Equivalent on Mar 24, 2023. The device falls under product code KIF (Resin, Root Canal Filling), a Class II device regulated under 21 CFR 872.3820.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 24, 2023
- Date Received
- Mar 22, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Resin, Root Canal Filling
- Device Class
- Class II
- Regulation Number
- 872.3820
- Review Panel
- DE
- Submission Type
- 510(k)