Djo Surgical

Djo Surgical holds 1 FDA 510(k) medical device clearance, cleared in 2009, with 1 FDA device recall on record.

FDA recalls by Djo Surgical

Z-1130-2014 — FMP X-alt Acetabular Liner This acetabular liner is intended for use with DJO Surgical hip systems. It is used with an acetabular shell to replicate the kinematics of a natural hip.Class II·Terminated·2014-02-07

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 Djo Surgical

K092873 — REVERSE SHOULDER PROSTHESISCode PHX·2009-10-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.

Top product codes for Djo Surgical

FDA recalls by Djo Surgical

Recent clearances by Djo Surgical