STRAUMANN GUIDED INSTRUMENTS— 510(k) K082532
Substantially EquivalentStraumann USA
FDA 510(k) clearance K082532 for STRAUMANN GUIDED INSTRUMENTS, Substantially Equivalent on 2008-10-21. Applicant: Straumann USA. Device class: 2.
Clearance details
- Applicant
- Straumann USA
- Product code
- Code DZI
- Device class
- Class 2
- Regulation
- 21 CFR 872.4120
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andover, MA, US
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