510(k) K121615
K121615 is an FDA 510(k) premarket notification submitted by Solco Biomedical Co., Ltd. for the device "4CIS VANE SPINE SYSTEM". The FDA issued a decision of Substantially Equivalent on August 15, 2012. The device falls under product code MNI (Orthosis, Spinal Pedicle Fixation), a Class II device regulated under 21 CFR 888.3070. Solco Biomedical Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 15, 2012
- Date Received
- June 1, 2012
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Orthosis, Spinal Pedicle Fixation
- Device Class
- Class II
- Regulation Number
- 888.3070
- Review Panel
- OR
- Submission Type