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NA

ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC. · Model 00-2700-042-00 · UDI-DI 00889024373587

HSS Prescription
3
510(k) clearances
3
Adverse events
0
Recalls
48
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.