K233601
- 510(k) number
- K233601
- Device name
- Fixone Meniscal Repair
- Applicant
- Aju Pharm Co., Ltd. KR
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2024-08-02
- Date received
- 2023-11-09
- 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: K233601.pdf
Official FDA record: K233601
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.