510(k) K062494

EBI OPTILOCK UPPER EXTREMITY PLATING SYSTEM by Ebi, L.P. — Product Code HRS

K062494 is an FDA 510(k) premarket notification submitted by Ebi, L.P. for the device "EBI OPTILOCK UPPER EXTREMITY PLATING SYSTEM". The FDA issued a decision of Substantially Equivalent on October 19, 2006. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Ebi, L.P. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 19, 2006
Date Received
August 25, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plate, Fixation, Bone
Device Class
Class II
Regulation Number
888.3030
Review Panel
OR
Submission Type