K243784
- 510(k) number
- K243784
- Device name
- Stryker Orthopaedics Hip Devices Labeling Update
- Applicant
- Howmedica Osteonics Corp., Dba Stryker Orthopaedics NJ · US
- Product code
- LPH — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Po
- Decision date
- 2025-02-06
- Date received
- 2024-12-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K243784.pdf
Official FDA record: K243784
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.