510(k) K923613

SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT by Synthes (Usa) — Product Code JDO

K923613 is an FDA 510(k) premarket notification submitted by Synthes (Usa) for the device "SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT". The FDA issued a decision of Substantially Equivalent on June 22, 1993. 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
June 22, 1993
Date Received
July 21, 1992
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