Straumann PrefGel— 510(k) K162311
Substantially EquivalentInstitut Straumann AG
FDA 510(k) clearance K162311 for Straumann PrefGel, Substantially Equivalent on 2017-03-07. Applicant: Institut Straumann AG. Device class: Unclassified.
Clearance details
- Applicant
- Institut Straumann AG
- Product code
- Code KJJ
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Basel, CH
Recent devices under product code KJJ
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