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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K202522

Synchro SELECT Guidewire · Stryker Neurovascular · decided 2020-09-25 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Synchro SELECTSSUP215PREStryker CorporationDQX MOF07613327508635
Synchro SELECTSSFT215PREStryker CorporationDQX MOF07613327508598
Synchro SELECTSSUP300STRStryker CorporationDQX MOF07613327508628
Synchro SELECTSSTD300PREStryker CorporationDQX MOF07613327508529
Synchro SELECTSSFT300STRStryker CorporationDQX MOF07613327508581
Synchro SELECTSSTD300STRStryker CorporationDQX MOF07613327508505
Synchro SELECTSSFT215STRStryker CorporationDQX MOF07613327508574
Synchro SELECTSSUP300PREStryker CorporationDQX MOF07613327508642
Synchro SELECTSSTD215PREStryker CorporationDQX MOF07613327508512
Synchro SELECTSSFT300PREStryker CorporationDQX MOF07613327508604
Synchro SELECTSSUP215STRStryker CorporationDQX MOF07613327508611
Synchro SELECTSSTD215STRStryker CorporationDQX MOF07613327508499