Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

KWI — Predicate Candidate Screening

34 FDA 510(k) clearances under this product code; the 50 most recent screened below.

126 daysmedian FDA review time
276 days90th percentile
34clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K260624Arthrex Radial Head Replacement SystemArthrex, Inc.2026-07-301540
K233592BioPoly Radial Head ImplantBioPoly, LLC2024-03-131260
K231188ALIGN Radial Head SystemSkeletal Dynamics, Inc.2023-09-281550
K213563DePuy Synthes Radial Head Replacement SystemDePuy Synthes2022-03-181290
K212872Avenger Radial Head SystemIn2bones USA, LLC2021-12-17990
K192754Avenger Radial Head SystemIn2bones USA, LLC2020-01-07990
K183618Revolution Radial HeadIgnite Orthopedics, Inc.2019-05-171420
K172688Align Radial Head SystemSkeletal Dynamics, LLC2017-12-221070
K132735AXIA RADIAL HEAD SYSTEMImds (Innovative MEdical Device Systems) - Leis ME2014-01-071260
K131845ACUMED ANATOMIC RADIAL HEAD SYSTEM, ACUMED ANATOMIC RADIAL HAcumed, LLC2013-09-301010
K112030SYNTHES RADIAL HEAD PROSTHESIS SYSTEMSynthes USA, LLC2012-06-193401
K092721ALIGN RADIAL HEAD SYSTEMSkeletal Dynamics, LLC2010-08-033331
K062898SBI LATERAL RHEAD IMPLANTSmall Bone Innovations, Inc.2006-11-13471
K060731EVOLVE MODULAR RADIAL HEADWrightmedicaltechnologyinc2006-04-19302
K051385EXPLOR MODULAR RADIAL HEAD REPLACEMENT DEVICEBiomet, Inc.2005-08-05701
K041858ACUMED ANATOMIC RADIAL HEAD SYSTEMAcumed, LLC2004-10-05880
K040611MODULAR RADIAL HEAD REPLACEMENT DEVICEBiomet, Inc.2004-06-04881
K032806KATALYST RADIAL HEAD IMPLANTKinetikos Medical, Inc.2004-04-162200
K032686ASCENSION MODULAR RADIAL HEADAscension Orthopedics, Inc.2003-10-22540
K030237KAPP CUSTOM RADIAL HEAD ELBOW IMPLANTKapp Surgical Instrument, Inc.2003-08-292180
K030384EVOLVE CERAMIC RADIAL HEAD IMPLANTWrightmedicaltechnologyinc2003-08-121880
K023604MODIFICATION TO RADIAL HEAD IMPLANTAvanta Orthopaedics, Inc.2002-11-27300
K012551LIVERPOOL RADIAL HEAD REPLACEMENT DEVICEBiomet, Inc.2002-01-301760
K011819RADIAL HEAD IMPLANTAvanta Orthopaedics, Inc.2001-06-1981
K002644RADIAL HEAD IMPLANTAvanta Orthopaedics, Inc.2000-11-20881
K994041TORNIER BIPOLAR RADIAL HEAD PROSTHESISTornier, Inc.2000-08-312760
K001385HOWMEDICA OSTEONICS RADIAL HEAD PROTHESISHowmedica Osteonics Corp.2000-07-27860
K000658ERS RADIAL HEAD REPLACEMENTDePuy Orthopaedics, Inc.2000-05-11730
K992220RADIAL HEAD PROSTHESISSmith & Nephew, Inc.2000-02-252390
K991915MODULAR RADIAL HEADWrightmedicaltechnologyinc1999-09-03882
K984290IMPLEX RADIAL HEAD REPLACEMENT SYSTEMImplex Corp.1999-06-011820
K982288RADIAL HEAD IMPLANTAvanta Orthopaedics, Inc.1998-09-08701
K944507METALLIC RADIAL HEAD IMPLANTSWrightmedicaltechnologyinc1995-07-133010
K885146CL UNIVERSAL HIP DEVICELima Intl. Corp.1989-04-241300

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda