510(k) K121615

4CIS VANE SPINE SYSTEM by Solco Biomedical Co., Ltd. — Product Code MNI

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