510(k) K100147

S4 CERVICAL OCCIPITAL PLATE SPINAL SYSTEM by Aesculap Implant System, Inc. — Product Code NKB

K100147 is an FDA 510(k) premarket notification submitted by Aesculap Implant System, Inc. for the device "S4 CERVICAL OCCIPITAL PLATE SPINAL SYSTEM". The FDA issued a decision of Substantially Equivalent on July 23, 2010. The device falls under product code NKB (Thoracolumbosacral Pedicle Screw System), a Class II device regulated under 21 CFR 888.3070. Aesculap Implant System, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 23, 2010
Date Received
January 19, 2010
Clearance Type
Special
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.