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Modulus
Nuvasive, Inc. · Model 1223245P2 · UDI-DI 00887517828613
1
510(k) clearances
23
Adverse events
0
Recalls
82
Facilities
Description
Modulus XLW, 12x22x45mm 5°
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Get your free API keyRead the docsData 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.
