510(k) K171595

M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System by Medacta International S.A. — Product Code OUR

K171595 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 Aug 2, 2017. 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
Aug 2, 2017
Date Received
May 31, 2017
Clearance Type
Traditional
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