K260037
- 510(k) number
- K260037
- Device name
- implantcast Packaging System Update
- Applicant
- Implantcast GmbH DE
- Product code
- LZO — Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Pol
- Decision date
- 2026-03-30
- Date received
- 2026-01-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 3.2 MB · U.S. public domain
Also available from FDA: K260037.pdf
Official FDA record: K260037
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.