510(k) K062872

SYNTHES (USA) PEDIATRIC LCP HIP PLATE SYSTEM by Synthes (Usa) — Product Code JDS

K062872 is an FDA 510(k) premarket notification submitted by Synthes (Usa) for the device "SYNTHES (USA) PEDIATRIC LCP HIP PLATE SYSTEM". The FDA issued a decision of Substantially Equivalent on March 13, 2007. The device falls under product code JDS (Nail, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Synthes (Usa) has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 13, 2007
Date Received
September 26, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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