K233259
- 510(k) number
- K233259
- Device name
- Xerosyn
- Applicant
- Xerothera, Inc. PA · US
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2024-06-21
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K233259.pdf
Official FDA record: K233259
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.