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

Clearance record K173717

Integra TITAN Reverse Shoulder System · Integra LifeSciences Corporation · decided 2018-06-21 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Titan Reverse Shoulder SystemBBS-0960-21STDSmith & Nephew, Inc.KWS PHX00885556863480
Titan Reverse Shoulder SystemBBS-0960-21SMLSmith & Nephew, Inc.KWS PHX00885556863473
Titan Reverse Shoulder SystemGBP-0960-030-25Smith & Nephew, Inc.KWS PHX00885556863732
Titan Reverse Shoulder SystemBBS-0960-21LRGSmith & Nephew, Inc.KWS PHX00885556863466
Titan Reverse Shoulder SystemGBP-0960-030-15Smith & Nephew, Inc.KWS PHX00885556863725