K232315
- 510(k) number
- K232315
- Device name
- Catalyst Bone Void Filler
- Applicant
- Ossdsign AB IE
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2023-09-15
- Date received
- 2023-08-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K232315.pdf
Official FDA record: K232315
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.