K233203
- 510(k) number
- K233203
- Device name
- Soft Tissue Augmentation Resorbable Matrix
- Applicant
- Collagen Matrix, Inc. NJ · US
- Product code
- NPL — Barrier, Animal Source, Intraoral
- Decision date
- 2024-05-01
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K233203.pdf
Official FDA record: K233203
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.