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LnK Spinal Fixation System

L&K BIOMED CO. ,LTD. · Model 1071-63550 · UDI-DI 08806189836902

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10
510(k) clearances
4,393
Adverse events (2 deaths)
0
Recalls
326
Facilities

Description

L&K Biomed Rod, Straight, CoCrMo 6.0x550mm 1EA

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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.