510(k) K032708
K032708 is an FDA 510(k) premarket notification submitted by Septodont for the device "PLASTALGIN AND PLASTALGIN ORTHO". The FDA issued a decision of Substantially Equivalent on November 20, 2003. The device falls under product code ELW (Material, Impression), a Class II device regulated under 21 CFR 872.3660. Septodont has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 20, 2003
- Date Received
- September 2, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Material, Impression
- Device Class
- Class II
- Regulation Number
- 872.3660
- Review Panel
- DE
- Submission Type