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VERTEX® Reconstruction System
Model 7756069 · MEDTRONIC SOFAMOR DANEK, INC. · DI 00613994448811
KWP — Appliance, Fixation, Spinal Interlaminal · Class II · 21 CFR 888.3050
UDILibrary device dossier · generated 2026-09-06 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (0)
No recalls linked in the loaded window.
Adverse-event reports — MAUDE (0)
Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-01
0
2.13
2019-02
0
1.87
2019-03
0
1.91
2019-04
0
1.98
2019-05
0
2.19
2019-06
0
2.19
2019-07
0
1.63
2019-08
0
2.5
2019-09
0
1.79
2019-10
0
1.85
2019-11
0
2.12
2019-12
0
1.54
2020-01
0
2.35
2020-02
0
2.32
2020-03
0
2.33
2020-04
0
1.45
2020-05
0
2.16
2020-06
0
1.93
2020-07
0
1.72
2020-08
0
1.83
2020-09
0
2.09
2020-10
0
2.38
2020-11
0
2.23
2020-12
0
2.07
2021-01
0
2.1
2021-02
0
1.83
2021-03
0
2.2
2021-04
0
2.05
2021-05
0
1.96
2021-06
0
1.88
2021-07
0
6.91
2021-08
0
1.89
2021-09
0
1.69
2021-10
0
2.28
2021-11
0
1.97
2021-12
0
1.97
2022-01
0
2.05
2022-02
0
1.91
2022-03
0
1.68
2022-04
0
1.78
2022-05
0
1.68
2022-06
0
1.95
2022-07
0
3.29
2022-08
0
1.88
2022-09
0
2.72
2022-10
0
1.43
2022-11
0
1.57
2022-12
0
1.94
2023-01
0
1.61
2023-02
0
1.78
2023-03
0
1.77
2023-04
0
2
2023-05
0
1.57
2023-06
0
1.64
2023-07
0
1.73
2023-08
0
1.34
2023-09
0
2.57
2023-10
0
2.44
2023-11
0
2.19
2023-12
0
1.63
2024-01
0
2.39
2024-02
0
2.14
2024-03
0
3.63
2024-04
0
1.73
2024-05
0
3.39
2024-06
0
2.23
2024-07
0
1.78
2024-08
0
1.79
2024-09
0
2.58
2024-10
0
2.27
2024-11
0
1.88
2024-12
0
1.76
2025-01
0
2.31
2025-02
0
2.45
2025-03
0
2.18
2025-04
0
2.25
2025-05
0
2.5
2025-06
0
2.29
2025-07
0
1.72
2025-08
0
1.96
2025-09
0
1.88
2025-10
0
1.93
2025-11
0
1.97
2025-12
0
2.27
2026-01
0
2.39
2026-02
0
2.4
2026-03
0
2.34
2026-04
0
1.83
2026-05
0
2.19
2026-06
0
4.25
This device (reports/month)Average device in KWP (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Predicate lineage
K090714 — cited as predicate by K121191, K121877, K123656, K163375, K181350, K223764
Lineage extracted from public 510(k) summary text (heuristic).
Manufacturer compliance record — MEDTRONIC SOFAMOR DANEK, INC.
NAI 2026-02-06 Medtronic Sofamor Danek USA Inc · 0 citations
NAI 2017-10-26 Medtronic Sofamor Danek USA, Inc · 0 citations
VAI 2015-11-03 Medtronic Sofamor Danek USA Inc · 0 citations
VAI 2015-10-23 Medtronic Sofamor Danek USA Inc · 1 citations
VAI 2014-03-11 Medtronic Sofamor Danek USA Inc · 0 citations
NAI 2013-07-15 Medtronic Sofamor Danek USA, Inc · 0 citations
NAI 2013-07-15 Medtronic Sofamor Danek USA Inc · 0 citations
VAI 2012-06-06 Medtronic Sofamor Danek USA Inc · 0 citations
NAI 2011-02-23 Medtronic Sofamor Danek Usa Inc · 0 citations
VAI 2010-08-06 Medtronic Sofamor Danek USA Inc · 0 citations
VAI 2010-03-04 Medtronic Sofamor Danek USA Inc · 0 citations
NAI 2010-02-25 Medtronic Sofamor Danek USA Inc · 0 citations