MULTILINK HYBRID ABUTMENT CEMENT— 510(k) K130436
Substantially EquivalentIvoclar Vivadent, AG
FDA 510(k) clearance K130436 for MULTILINK HYBRID ABUTMENT CEMENT, Substantially Equivalent on 2013-08-20. Applicant: Ivoclar Vivadent, AG. Device class: 2.
Clearance details
- Applicant
- Ivoclar Vivadent, AG
- Product code
- Code EMA
- Device class
- Class 2
- Regulation
- 21 CFR 872.3275
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Amherst, NY, US
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