510(k) K120740
K120740 is an FDA 510(k) premarket notification submitted by Fournitures Hospitalieres Industrie for the device "COLS® FIXATION SYSTEM". The FDA issued a decision of Substantially Equivalent on Mar 5, 2013. The device falls under product code MBI (Fastener, Fixation, Nondegradable, Soft Tissue), a Class II device regulated under 21 CFR 888.3040. Fournitures Hospitalieres Industrie has 23 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 5, 2013
- Date Received
- Mar 12, 2012
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Fastener, Fixation, Nondegradable, Soft Tissue
- Device Class
- Class II
- Regulation Number
- 888.3040
- Review Panel
- OR
- Submission Type
- 510(k)