K250989
- 510(k) number
- K250989
- Device name
- Stryker and Serf hip devices
- Applicant
- Howmedica Osteonics Corp (Dba Stryker Orthopaedics) NJ · US
- Product code
- LPH — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Po
- Decision date
- 2025-07-25
- Date received
- 2025-03-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K250989.pdf
Official FDA record: K250989
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.