AccuPlan System
Medcad · Model ZB-KT030-H · UDI-DI 00810007632124
1
510(k) clearances
226
Adverse events (1 deaths)
0
Recalls
35
Facilities
Description
ORTHOPEDIC, TITANIUM HYBRID SURGICAL GUIDE, GRAFT
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.