510(k) K200868
K200868 is an FDA 510(k) premarket notification submitted by Biofusion Medical for the device "SI-Restore Sacroiliac Joint Fixation System". The FDA issued a decision of Substantially Equivalent on Apr 17, 2020. The device falls under product code OUR (Sacroiliac Joint Fixation), a Class II device regulated under 21 CFR 888.3040. Biofusion Medical has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 17, 2020
- Date Received
- Apr 1, 2020
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sacroiliac Joint Fixation
- Device Class
- Class II
- Regulation Number
- 888.3040
- Review Panel
- OR
- Submission Type
- 510(k)
sacroiliac joint fusion