K231672
- 510(k) number
- K231672
- Device name
- S1
- Applicant
- Medpark Co., Ltd. KR
- Product code
- NPM — Bone Grafting Material, Animal Source
- Decision date
- 2023-10-13
- Date received
- 2023-06-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K231672.pdf
Official FDA record: K231672
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.