510(k) K163060
K163060 is an FDA 510(k) premarket notification submitted by Southern Implants (Pty), Ltd. for the device "Deep Conical (DC) Implants and Accessories". The FDA issued a decision of Substantially Equivalent on Jun 13, 2017. The device falls under product code DZE (Implant, Endosseous, Root-Form), a Class II device regulated under 21 CFR 872.3640. Southern Implants (Pty), Ltd. has 18 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 13, 2017
- Date Received
- Nov 1, 2016
- 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)