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

Clearance record K211729

Comprehensive® Convertible Glenoid - Vivacit-E Liner · Biomet Manufacturing Corp · decided 2021-11-04 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Comprehensive® Shoulder System110035767Biomet Orthopedics, LLCKWS KWT MBF PAO PHX00887868249334