Synchro SELECT Guidewire
K-Number: K202522 · 2020-09-25
ApplicantStryker Neurovascular
Decision Date2020-09-25
Product CodeMOF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Synchro SELECT Guidewire is a medical device manufactured by Stryker Neurovascular. It received FDA 510(k) clearance on 2020-09-25 under approval number K202522. The device is classified under product code MOF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Synchro SELECT Guidewire?
Synchro SELECT Guidewire is a medical device that received FDA 510(k) clearance on 2020-09-25. It is manufactured by Stryker Neurovascular. The 510(k) number is K202522.
When was Synchro SELECT Guidewire approved by the FDA?
Synchro SELECT Guidewire received FDA 510(k) clearance on 2020-09-25, under approval number K202522.
What company makes Synchro SELECT Guidewire?
Synchro SELECT Guidewire is manufactured by Stryker Neurovascular.
What is the FDA product code for Synchro SELECT Guidewire?
The FDA product code for Synchro SELECT Guidewire is MOF.
Related Clinical Trials
Other Devices by Stryker Neurovascular
Related Devices (Code: MOF)
K163154Traxcess 7 Mini XSoft GuidewireMicroVention, Inc.
K161912ASAHI Neurovascular Guide Wire: ASAHI CHIKAI black 14 soft tipAsahi Intecc Co., Ltd.
K161803Traxcess .007 Mini GuidewireMicroVention, Inc.
K160659ASAHI CHIKAI Neurovascular Guide Wire (Round Curve)Asahi Intecc Co., Ltd.
K171613ASAHI Neurovasulature Guide Wire: ASAHI CHIKAI black 18 soft tipAsahi Intecc Co., Ltd.
K182337HYBRID GuidewireBalt USA, LLC
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.