510(k) K120453
K120453 is an FDA 510(k) premarket notification submitted by 3M Espe Dental Products for the device "FILTEK BULK FILL FLOWABLE RESTORATIVE". The FDA issued a decision of Substantially Equivalent on March 19, 2012. The device falls under product code EBF (Material, Tooth Shade, Resin), a Class II device regulated under 21 CFR 872.3690. 3M Espe Dental Products has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 19, 2012
- Date Received
- February 14, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Material, Tooth Shade, Resin
- Device Class
- Class II
- Regulation Number
- 872.3690
- Review Panel
- DE
- Submission Type