510(k) K260106
K260106 is an FDA 510(k) premarket notification submitted by Flower Orthopedics Corporation DBA Conventus Flower Orthoped for the device "OsteoCoil GT Active Compression System". The FDA issued a decision of Substantially Equivalent on August 24, 2026. The device falls under product code HWC (Screw, Fixation, Bone), a Class II device regulated under 21 CFR 888.3040.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 24, 2026
- Date Received
- January 14, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Screw, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3040
- Review Panel
- OR
- Submission Type