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Journey II

Smith & Nephew, Inc. · Model E0015754-2 · UDI-DI 00885556707166

LHX Prescription
4
510(k) clearances
102
Adverse events
1
Recalls
1
Facilities

Description

TIBIAL CUTTING GUIDE - RIGHT 3 DEGREE

Recalls

DateFirmReason
2010-01-18Stryker SpineStryker Spine received reports of packaging failures during shipping for the Jam Shidi instruments, which may compromise the sterility of the product.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.