K260106
- 510(k) number
- K260106
- Device name
- OsteoCoil GT Active Compression System
- Applicant
- Flower Orthopedics Corporation DBA Conventus Flower Orthoped PA · US
- Product code
- HWC — Screw, Fixation, Bone
- Decision date
- 2026-08-24
- Date received
- 2026-01-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K260106.pdf
Official FDA record: K260106
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.