510(k) K172786
K172786 is an FDA 510(k) premarket notification submitted by Miami Device Solutions, LLC for the device "MDS Plating System". The FDA issued a decision of Substantially Equivalent on December 8, 2017. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Miami Device Solutions, LLC has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 8, 2017
- Date Received
- September 15, 2017
- 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