STRAUMANN MEMBRAGEL— 510(k) K082111
Substantially EquivalentInstitut Straumann AG
FDA 510(k) clearance K082111 for STRAUMANN MEMBRAGEL, Substantially Equivalent on 2009-05-22. Applicant: Institut Straumann AG. Device class: 2.
Clearance details
- Applicant
- Institut Straumann AG
- Product code
- Code NPK
- Device class
- Class 2
- Regulation
- 21 CFR 872.3930
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andover, MA, US
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