510(k) K053629
K053629 is an FDA 510(k) premarket notification submitted by Kj Meditech for the device "ANCHOR PLUS/NEO ANCHOR PLUS". The FDA issued a decision of Substantially Equivalent on May 31, 2006. 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
- May 31, 2006
- Date Received
- Dec 29, 2005
- 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)