510(k) K252661
K252661 is an FDA 510(k) premarket notification submitted by Fusion Innovations, LLC for the device "SternaFuse Ti Fixation System". The FDA issued a decision of Substantially Equivalent on Nov 19, 2025. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Fusion Innovations, LLC has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 19, 2025
- Date Received
- Aug 22, 2025
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Plate, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type