K232602
- 510(k) number
- K232602
- Device name
- 3DMatrix Surgical Mesh
- Applicant
- Printbio, Inc. NY · US
- Product code
- OXF — Mesh, Surgical, Absorbable, Plastic And Reconstructi
- Decision date
- 2024-05-23
- Date received
- 2023-08-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232602.pdf
Official FDA record: K232602
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.