510(k) K113388
K113388 is an FDA 510(k) premarket notification submitted by Citieffe for the device "CITIEFFE-TITANIUM CANNULATED SCREW". The FDA issued a decision of Substantially Equivalent on June 5, 2012. The device falls under product code HWC (Screw, Fixation, Bone), a Class II device regulated under 21 CFR 888.3040. Citieffe has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 5, 2012
- Date Received
- November 16, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Screw, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3040
- Review Panel
- OR
- Submission Type