510(k) K964259

SYNTHES (USA) DDHS/DCS SYSTEM MODIFICATION by Synthes (Usa) — Product Code JDO

K964259 is an FDA 510(k) premarket notification submitted by Synthes (Usa) for the device "SYNTHES (USA) DDHS/DCS SYSTEM MODIFICATION". The FDA issued a decision of Substantially Equivalent on January 9, 1997. The device falls under product code JDO (Device, Fixation, Proximal Femoral, Implant), 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
January 9, 1997
Date Received
October 25, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Fixation, Proximal Femoral, Implant
Device Class
Class II
Regulation Number
888.3030
Review Panel
OR
Submission Type