510(k) K082651
K082651 is an FDA 510(k) premarket notification submitted by Southern Implants, Inc. for the device "ENDOSSEOUS DENTAL IMPLANT SYSTEM". The FDA issued a decision of Substantially Equivalent on December 22, 2008. The device falls under product code DZE (Implant, Endosseous, Root-Form), a Class II device regulated under 21 CFR 872.3640. Southern Implants, Inc. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 22, 2008
- Date Received
- September 12, 2008
- 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