K232592
- 510(k) number
- K232592
- Device name
- CITRELOCK® DUO
- Applicant
- Acuitive Technologies, Inc. NJ · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2023-09-20
- Date received
- 2023-08-25
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K232592.pdf
Official FDA record: K232592
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.