Epic Extremity, LLC
Epic Extremity, LLC holds FDA 510(k) medical device clearances, first cleared 2016, most recent 2019, with 2 FDA device recalls on record.
Top product codes for Epic Extremity, LLC
FDA recalls by Epic Extremity, LLC
- Z-1874-2018 — Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)
- Z-1875-2018 — Epic Extremity Plate System,10x10 Plate Caddy, Part 2111-1010 with 2.7 and 3.5mm Non-Locking Screw (2001-27XX-N & 2001-35XX-N)
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Epic Extremity, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.