510(k) K051557

TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS by Smith & Nephew, Inc. — Product Code JDS

K051557 is an FDA 510(k) premarket notification submitted by Smith & Nephew, Inc. for the device "TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS". The FDA issued a decision of Substantially Equivalent on June 30, 2005. The device falls under product code JDS (Nail, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Smith & Nephew, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 30, 2005
Date Received
June 13, 2005
Clearance Type
Special
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