Atlas FDA

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

Degen Medical · Predicate Candidate Screening

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

127 daysmedian FDA review time
222 days90th percentile
16clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K251829DeGen Medical Patient Specific Implant (PSI) SystemDegen Medical2025-12-081780
K252737DeGen Medical Latitude-C AM Cervical Interbody Fusion SystemDegen Medical2025-10-10430
K250667DeGen Medical Patient Specific Implant (PSI) SystemDegen Medical2025-04-04300
K241077DeGen Medical Patient Specific Implant (PSI) SystemDegen Medical2024-10-291930
K231199Solar Lumbar Interbody Fusion SystemDegen Medical2023-06-16500
K223418DeGen Impulse AM™ SystemDegen Medical2023-03-171270
K213918DeGen Navigated InstrumentationDegen Medical2022-02-09560
K213901Cyclops™ Anterior Cervical Plate SystemDegen Medical2022-01-07240
K210090Impulse AM Interbody Fusion SystemDegen Medical2021-08-302290
K203816DeGen Navigated InstrumentationDegen Medical2021-04-02940
K201287Impulse Interbody Fusion SystemDegen Medical2020-12-222220
K173814DeGen Medical E3 MIS Pedicle Screw SystemDegen Medical2018-01-29450
K160926F1 MPS Modular Pedicle Screw SystemDegen Medical2016-06-28850
K151496Latitude-C Cervical Interbody Spacer SystemDegen Medical2015-12-151950
K150759Hyper-C Anterior Cervical Plate SystemDegen Medical2015-07-281270
K142531F1-Modular Pedicle Screw SystemDegen Medical2015-03-201920

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