Atlas FDA

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

DePuy Synthes — Predicate Candidate Screening

19 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

90 daysmedian FDA review time
263 days90th percentile
19clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K233696DePuy Synthes Retrograde Femoral Nail Advanced SystemDePuy Synthes2024-08-012580
K233256Robotic Integration InstrumentsDePuy Synthes2024-06-172630
K233255CROSSNAV Navigation Enabled InstrumentsDePuy Synthes2024-06-172630
K233254TELIGEN System Navigation Ready InstrumentsDePuy Synthes2024-06-142600
K233665DePuy Synthes VOLT Mini Fragment Plating System, DePuy SynthDePuy Synthes2024-03-211270
K231922DEPUY SYNTHES MAXFRAME AUTOSTRUT SystemDePuy Synthes2023-07-26270
K221809DePuy Synthes 3.5mm Intrapelvic Acetabular SystemDePuy Synthes2022-09-20900
K213563DePuy Synthes Radial Head Replacement SystemDePuy Synthes2022-03-181290
K211051DePuy Synthes 2.7mm Straight and 2.7mm Adaption Plates (ModuDePuy Synthes2021-06-02550
K203414DePuy Synthes 2.7mm VA LCP Clavicle Plate System, DePuy SyntDePuy Synthes2020-12-16270
K201959DePuy Synthes 2.7mm VA LCP Clavicle Hook Plate SystemDePuy Synthes2020-09-11590
K201321DePuy Synthes 2.7mm VA LCP Clavicle Plate SystemDePuy Synthes2020-07-24671
K190750DePuy Synthes Plates and Screws PortfolioDePuy Synthes2019-06-21880
K190409MatrixRIB Fixation SystemDePuy Synthes2019-05-03710
K182783DePuy Synthes Trauma Orthopedic Nail ImplantsDePuy Synthes2018-12-26860
K172872DePuy Synthes Femoral Neck SystemDePuy Synthes2018-03-051650
K162124Synthes 4.5mm VA-LCP Curved Condylar Plate System Line ExtenDePuy Synthes2017-03-292400
K163046DePuy Synthes 2.4/2.7mm VA LCP Two-Column Volar Distal RadiuDePuy Synthes2017-02-091000
K792352SYNTHES CERVICAL VERTABRAE PLATESDePuy Synthes1979-12-06170

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