Cytoplast Titanium-Reinforced PTFE Membranes— 510(k) K201187
Substantially EquivalentOsteogenics Biomedical, Inc.
FDA 510(k) clearance K201187 for Cytoplast Titanium-Reinforced PTFE Membranes, Substantially Equivalent on 2021-01-23. Applicant: Osteogenics Biomedical, Inc.. Device class: 2.
Clearance details
- Applicant
- Osteogenics Biomedical, Inc.
- 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
- Lubbock, TX, US
Recent devices under product code NPK
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