510(k) K122664
K122664 is an FDA 510(k) premarket notification submitted by Zuga Medical, Inc. for the device "ZUGA DENTAL IMPLANT SYSTEM". The FDA issued a decision of Substantially Equivalent on Apr 30, 2013. The device falls under product code DZE (Implant, Endosseous, Root-Form), a Class II device regulated under 21 CFR 872.3640. Zuga Medical, Inc. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 30, 2013
- Date Received
- Aug 31, 2012
- 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)