K241296
- 510(k) number
- K241296
- Device name
- Gaudi Proximal Humerus Plate
- Applicant
- Netbiologics, LLC FL · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2024-07-23
- Date received
- 2024-05-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.0 MB · U.S. public domain
Also available from FDA: K241296.pdf
Official FDA record: K241296
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.