510(k) K101997
K101997 is an FDA 510(k) premarket notification submitted by Ellipse Technologies, Inc. for the device "ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM". The FDA issued a decision of Substantially Equivalent on July 12, 2011. 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
- July 12, 2011
- Date Received
- July 15, 2010
- 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