K233208
- 510(k) number
- K233208
- Device name
- NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium
- Applicant
- Nobel Biocare AB SE
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-01-24
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K233208.pdf
Official FDA record: K233208
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.