510(k) K181331
K181331 is an FDA 510(k) premarket notification submitted by Juvora, Ltd. for the device "JUVORA Oyster White Dental Disc, CERAMILL PEEK by JUVORA, Oyster White". The FDA issued a decision of Substantially Equivalent on Dec 21, 2018. The device falls under product code EBI (Resin, Denture, Relining, Repairing, Rebasing), a Class II device regulated under 21 CFR 872.3760. Juvora, Ltd. has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 21, 2018
- Date Received
- May 21, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Resin, Denture, Relining, Repairing, Rebasing
- Device Class
- Class II
- Regulation Number
- 872.3760
- Review Panel
- DE
- Submission Type
- 510(k)