510(k) K141023

PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM by Ellipse Technologies, Inc. — Product Code HSB

K141023 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 May 20, 2014. 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
May 20, 2014
Date Received
April 21, 2014
Clearance Type
Special
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