510(k) K103577
K103577 is an FDA 510(k) premarket notification submitted by Trinon Titanium GmbH for the device "TRINON Q & Q3 IMPLANT SYSTEM". The FDA issued a decision of Substantially Equivalent on Jul 3, 2012. The device falls under product code DZE (Implant, Endosseous, Root-Form), a Class II device regulated under 21 CFR 872.3640. Trinon Titanium GmbH has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 3, 2012
- Date Received
- Dec 6, 2010
- 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)