510(k) K964259
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