K233089
- 510(k) number
- K233089
- Device name
- NeoSpan® Compression Implant System
- Applicant
- In2bones USA, LLC TN · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2024-05-24
- Date received
- 2023-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K233089.pdf
Official FDA record: K233089
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.