510(k) K201827
K201827 is an FDA 510(k) premarket notification submitted by Pro3Dure Medical GmbH for the device "GR-17 Resin System". The FDA issued a decision of Substantially Equivalent on November 5, 2020. The device falls under product code EBG (Crown And Bridge, Temporary, Resin), a Class II device regulated under 21 CFR 872.3770. Pro3Dure Medical GmbH has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 5, 2020
- Date Received
- July 2, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Crown And Bridge, Temporary, Resin
- Device Class
- Class II
- Regulation Number
- 872.3770
- Review Panel
- DE
- Submission Type