ClearanceBrief
510(k) K031572 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

ZMR HIP SYSTEM-XL, MODELS 9921, 9922 AND 9923

ApplicantZimmer, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jun 24, 2003
ReceivedMay 20, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K031572

DateFirm and productCodeLinked 510(k)
Mar 20, 2017Zimmer Biomet, Inc.
Xl por st 24.0x220mm, bowed, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
Terminated
LPHNone listed
Mar 20, 2017Zimmer Biomet, Inc.
Xl por st 25.5x220mm, bowed\, bowed, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
Terminated
LPHNone listed
Dec 1, 2011Zimmer Inc.
Zimmer ZMR Hip System Instructions for Use, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compression Nut, Splined Straight
Terminated
LPHNone listed
Dec 1, 2011Zimmer Inc.
ZMR Porous Revision Hip Prosthesis Surgical Technique, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compression Nut, Spline
Terminated
LPHNone listed
Dec 1, 2011Zimmer Inc.
ZMR Crossover Instrumentation, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compression Nut, Splined Straight Stem, Taper S
Terminated
LPHNone listed
Dec 1, 2011Zimmer Inc.
ZMR Over the Junction Instruments for Revision, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compression Nut, Splined Strai
Terminated
LPHNone listed

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