ClearanceBrief
510(k) K071723 ยท KWA Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)

ZIMMER POROLOCK MIS STEM

ApplicantZimmer GmbH, Warsaw IN, US
DecisionSubstantially Equivalent, Mar 7, 2008
ReceivedJun 25, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071723

DateFirm and productCodeLinked 510(k)
Oct 10, 2019Zimmer Biomet, Inc.
Fitmore Hip Stem, hip prosthesis, various sizes, Item Nos. 0100551102 0100551103 0100551104 0100551105 0100551106 0100551107 0100551108 0100551109 0100551110 0100551111 0100551112 0100551113 010055111
Terminated
LZONone listed
Nov 6, 2012Zimmer, Inc.
Fitmore" Hip Stem
Terminated
KWANone listed

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