K233355
- 510(k) number
- K233355
- Device name
- Cypris eXact Suturing System
- Applicant
- Cypris Medical IL · US
- Product code
- GAW — Suture, Nonabsorbable, Synthetic, Polypropylene
- Decision date
- 2024-01-12
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233355.pdf
Official FDA record: K233355
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.