510(k) K173051
K173051 is an FDA 510(k) premarket notification submitted by Orthofix Srl for the device "Orthofix MJ-FLEX THE NEW METAIZEAU NAIL". The FDA issued a decision of Substantially Equivalent on Nov 16, 2017. The device falls under product code HTY (Pin, Fixation, Smooth), a Class II device regulated under 21 CFR 888.3040. Orthofix Srl has 97 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 16, 2017
- Date Received
- Sep 28, 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)