510(k) K030087

SPINAL CONCEPTS, INC. BACFIX TI SPINAL SYSTEM by Spinal Concepts, Inc. — Product Code NKB

K030087 is an FDA 510(k) premarket notification submitted by Spinal Concepts, Inc. for the device "SPINAL CONCEPTS, INC. BACFIX TI SPINAL SYSTEM". The FDA issued a decision of Substantially Equivalent on July 17, 2003. The device falls under product code NKB (Thoracolumbosacral Pedicle Screw System), a Class II device regulated under 21 CFR 888.3070. Spinal Concepts, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 17, 2003
Date Received
January 9, 2003
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Thoracolumbosacral Pedicle Screw System
Device Class
Class II
Regulation Number
888.3070
Review Panel
OR
Submission Type

Intended to provide immobilization and stabilization of spinal segments in thoracic, lumbar, and sacral spine as an adjunct to fusion.