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LLD™ #3

Spectranetics Corporation · Model 518-023AA · UDI-DI 00813132020798

DRB Prescription
1
510(k) clearances
1,275
Adverse events (77 deaths)
0
Recalls
39
Facilities

Description

Lead Locking Device (LLD™ #3)

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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.