510(k) K170326
K170326 is an FDA 510(k) premarket notification submitted by Arthrex, Inc. for the device "dynaMX Intramedullary Implant". The FDA issued a decision of Substantially Equivalent on Jul 20, 2017. The device falls under product code HTY (Pin, Fixation, Smooth), a Class II device regulated under 21 CFR 888.3040. Arthrex, Inc. has 352 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 20, 2017
- Date Received
- Feb 2, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pin, Fixation, Smooth
- Device Class
- Class II
- Regulation Number
- 888.3040
- Review Panel
- OR
- Submission Type
- 510(k)