AnyPlus® Spinal Fixation System
K-Number: K172546 · 2017-10-23
ApplicantGS Medical Co., Ltd.
Decision Date2017-10-23
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
AnyPlus® Spinal Fixation System is a medical device manufactured by GS Medical Co., Ltd.. It received FDA 510(k) clearance on 2017-10-23 under approval number K172546. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the AnyPlus® Spinal Fixation System?
AnyPlus® Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2017-10-23. It is manufactured by GS Medical Co., Ltd.. The 510(k) number is K172546.
When was AnyPlus® Spinal Fixation System approved by the FDA?
AnyPlus® Spinal Fixation System received FDA 510(k) clearance on 2017-10-23, under approval number K172546.
What company makes AnyPlus® Spinal Fixation System?
AnyPlus® Spinal Fixation System is manufactured by GS Medical Co., Ltd..
What is the FDA product code for AnyPlus® Spinal Fixation System?
The FDA product code for AnyPlus® Spinal Fixation System is NKB.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.