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

Clearance record K200398

AxSOS 3 AF System and AxSOS 3 Ti System · Stryker GmbH · decided 2020-06-05 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
AxSOS 3630112SStryker GmbHHRS HWC07613327410099
AxSOS 3630114Stryker GmbHHRS HWC07613327410082
AxSOS 3630111SStryker GmbHHRS HWC07613327410570
AxSOS 3630103Stryker GmbHHRS HWC07613327410440
AxSOS 3630103SStryker GmbHHRS HWC07613327410518
AxSOS 3630112Stryker GmbHHRS HWC07613327410662
AxSOS 3630102Stryker GmbHHRS HWC07613327410396
AxSOS 3630104Stryker GmbHHRS HWC07613327410532
AxSOS 3630102SStryker GmbHHRS HWC07613327410457
AxSOS 3630101SStryker GmbHHRS HWC07613327411928
AxSOS 3630113Stryker GmbHHRS HWC07613327410044
AxSOS 3630111Stryker GmbHHRS HWC07613327410754
AxSOS 3630104SStryker GmbHHRS HWC07613327410747
AxSOS 3630113SStryker GmbHHRS HWC07613327410259
AxSOS 3630101Stryker GmbHHRS HWC07613327410303
AxSOS 3630114SStryker GmbHHRS HWC07613327410181