510(k) K143622
K143622 is an FDA 510(k) premarket notification submitted by Mx Orthopedics, Corp. for the device "dynaMX Compression Staple". The FDA issued a decision of Substantially Equivalent on Jun 17, 2015. The device falls under product code JDR (Staple, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Mx Orthopedics, Corp. has 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 17, 2015
- Date Received
- Dec 22, 2014
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Staple, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type
- 510(k)