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Continuum® Trilogy® Allofit®

Zimmer, Inc. · Model 00-8732-015-36 · UDI-DI 00889024147751

OQHOQGLPHOQILZOJDI Prescription
2
510(k) clearances
8
Adverse events
0
Recalls
55
Facilities

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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.