510(k) K160325
K160325 is an FDA 510(k) premarket notification submitted by Ellipse Technologies, Inc. for the device "PRECICE Intramedullary Limb Lengthening System". The FDA issued a decision of Substantially Equivalent on April 4, 2016. The device falls under product code HSB (Rod, Fixation, Intramedullary And Accessories), a Class II device regulated under 21 CFR 888.3020. Ellipse Technologies, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 4, 2016
- Date Received
- February 5, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Rod, Fixation, Intramedullary And Accessories
- Device Class
- Class II
- Regulation Number
- 888.3020
- Review Panel
- OR
- Submission Type