K254253
- 510(k) number
- K254253
- Device name
- LOQTEQ® VA Proximal Humerus Plate 3.5
- Applicant
- Aap Implantate AG DE
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2026-03-24
- Date received
- 2025-12-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K254253.pdf
Official FDA record: K254253
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.