K240418
- 510(k) number
- K240418
- Device name
- Stryker Orthopaedics Hip Systems Labeling Update
- Applicant
- Howmedica Osteonics Corp., Dba Stryker Orthopaedics NJ · US
- Product code
- JDI — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Ce
- Decision date
- 2024-04-12
- Date received
- 2024-02-13
- 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: K240418.pdf
Official FDA record: K240418
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.