K241992
- 510(k) number
- K241992
- Device name
- Catalyft LS Expandable Interbody System
- Applicant
- Medtronic Sofamor Danek USA, Inc. TN · US
- Product code
- OVD — Intervertebral Fusion Device With Integrated Fixatio
- Decision date
- 2024-10-28
- Date received
- 2024-07-08
- 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: K241992.pdf
Official FDA record: K241992
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.