510(k) K173410
K173410 is an FDA 510(k) premarket notification submitted by Institut Straumann AG for the device "n!ce for Planmill". The FDA issued a decision of Substantially Equivalent on Nov 14, 2017. The device falls under product code EIH (Powder, Porcelain), a Class II device regulated under 21 CFR 872.6660. Institut Straumann AG has 91 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 14, 2017
- Date Received
- Nov 1, 2017
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Powder, Porcelain
- Device Class
- Class II
- Regulation Number
- 872.6660
- Review Panel
- DE
- Submission Type
- 510(k)