510(k) K203671
K203671 is an FDA 510(k) premarket notification submitted by Medacta International S.A. for the device "M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System". The FDA issued a decision of Substantially Equivalent on Jan 13, 2021. The device falls under product code OUR (Sacroiliac Joint Fixation), a Class II device regulated under 21 CFR 888.3040. Medacta International S.A. has 207 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 13, 2021
- Date Received
- Dec 16, 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