K241356
- 510(k) number
- K241356
- Device name
- Fine Osteotomy
- Applicant
- Bodycad Laboratories, Inc. CA
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2024-09-05
- Date received
- 2024-05-14
- 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: K241356.pdf
Official FDA record: K241356
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.