510(k) K062367
K062367 is an FDA 510(k) premarket notification submitted by Micerium S.P.A. for the device "MINISCREWS ANCHORING SYSTEM, M.A.S.". The FDA issued a decision of Substantially Equivalent on Dec 8, 2006. The device falls under product code DZE (Implant, Endosseous, Root-Form), a Class II device regulated under 21 CFR 872.3640. Micerium S.P.A. has 5 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 8, 2006
- Date Received
- Aug 14, 2006
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Implant, Endosseous, Root-Form
- Device Class
- Class II
- Regulation Number
- 872.3640
- Review Panel
- DE
- Submission Type
- 510(k)