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nvp

NVision Biomedical Technologies, Inc. · Model PL-1000T-601 · UDI-DI 00814008021130

HXG
1
510(k) clearances
161
Adverse events (7 deaths)
0
Recalls
234
Facilities

Description

Instrument, Tamp Straight, Posterior Lumbar Interbody Fusion System (PLIF)

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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.