510(k) K101956
K101956 is an FDA 510(k) premarket notification submitted by Straumann USA (On Behalf of Institut Straumann Ag) for the device "STRAUMANN MEMBRAGEL". The FDA issued a decision of Substantially Equivalent on December 16, 2010. The device falls under product code NPK (Barrier, Synthetic, Intraoral), a Class II device regulated under 21 CFR 872.3930. Straumann USA (On Behalf of Institut Straumann Ag) has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 16, 2010
- Date Received
- July 12, 2010
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Barrier, Synthetic, Intraoral
- Device Class
- Class II
- Regulation Number
- 872.3930
- Review Panel
- DE
- Submission Type
A synthetic dental barrier is a synthetic material device, such as ptfe, intended to aid in guided tissue and/or bone regeneration procedures and to act as a stable barrier for the containment of bone graft materials.