ClearanceBrief
510(k) K170593 ยท OLO Orthopedic Stereotaxic Instrument

Mako Total Hip Application

ApplicantMako Surgical Corp., Fort Lauderdale FL, US
DecisionSubstantially Equivalent, Apr 18, 2017
ReceivedFeb 28, 2017
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K170593

DateFirm and productCodeLinked 510(k)
Dec 27, 2017Mako Surgical Corporation
Makoplasty RIO Standard System; Ethernet to Fiber Optic Converter Catalog # 200933 Product Usage: The Partial Knee Application (PKA), for use with the Mako System, is indicated for use in surgical kn
Terminated
OLONone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.