510(k) Report

Devices descending from K991753

17 later devices reach Maxim Removable Molded Poly Tibia through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K060525Vanguard Removable Molded Poly TibiaBiomet Manufacturing Corp2006163
+2K171054Biomet Knee Joint Replacement ProsthesesBiomet, Inc.201754
+2K102580Vanguard Removable Molded Poly TibiaBiomet Manufacturing Corp20119—
+3K181947Persona Revision Knee SystemZimmer, Inc.201841
+3K142814Biomet Orthopaedic Salvage System (OSSTM) - Proximal Femoral & Hybrid TibialBiomet Manufacturing, LLC201516
+3K122160Vanguard XP Knee SystemBiomet Manufacturing Corp2013612
+4K253515Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and AugmentsBiomet Orthopedics, Inc.20260—
+4K243724Persona® Revision Knee System (Persona Revision SoluTion™ Femoral Components)Zimmer, Inc.20250—
+4K210829Persona Revision Knee System Femoral Metaphyseal ConesZimmer, Inc.20210—
+4K191625Persona Revision Knee SystemZimmer, Inc.201911
+4K190068Vanguard XP Knee SystemZimmer, Inc.20190—
+4K153657Vanguard XP Knee SystemBiomet, Inc.201611
+4K143635KINETIS Total Knee SystemMako Surgical20150—
+4K141407Vanguard XP Femoral Component (Gen II)/Vanguard XP Femoral TrialBiomet, Inc.201421
+4K140257Signature Planner, Signature GuidesMaterialise NV20140—
+4K132873Vanguard XP Knee SystemBiomet, Inc.2013322
+5K210551Persona Revision Knee SystemZimmer, Inc.202101