510(k) K171769
K171769 is an FDA 510(k) premarket notification submitted by Straumann USA, LLC (On Behalf Of Institut Straumann Ag) for the device "Straumann PURE Ceramic Implants". The FDA issued a decision of Substantially Equivalent on Nov 14, 2017. The device falls under product code DZE (Implant, Endosseous, Root-Form), a Class II device regulated under 21 CFR 872.3640. Straumann USA, LLC (On Behalf Of Institut Straumann Ag) has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 14, 2017
- Date Received
- Jun 14, 2017
- 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)