510(k) K851717
K851717 is an FDA 510(k) premarket notification submitted by Artiberia for the device "880/1 TO 890/4 VARIOUS TYPES OF PERIOTEAL ELEVATOR". The FDA issued a decision of Substantially Equivalent on June 14, 1985. The device falls under product code EMJ (Elevator, Surgical, Dental), a Class I device regulated under 21 CFR 872.4565. Artiberia has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 14, 1985
- Date Received
- April 25, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Elevator, Surgical, Dental
- Device Class
- Class I
- Regulation Number
- 872.4565
- Review Panel
- DE
- Submission Type