510(k) K033630
K033630 is an FDA 510(k) premarket notification submitted by Rhein 83 Srl for the device "MODIFICATION OF: SPHERO FLEX, PIVOT FLEX, AND SPHERO BLOCK". The FDA issued a decision of Substantially Equivalent on Apr 21, 2004. The device falls under product code DZE (Implant, Endosseous, Root-Form), a Class II device regulated under 21 CFR 872.3640.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 21, 2004
- Date Received
- Nov 17, 2003
- Clearance Type
- Special
- 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)