Print-ready dossier — use your browser's print dialog to save as PDF.
POWEREASE™ Instruments
Model 2342425 · MEDTRONIC SOFAMOR DANEK, INC. · DI 00643169013100
GWF — Stimulator, Electrical, Evoked Response · Class II · 21 CFR 882.1870
HBE — Drills, Burrs, Trephines & Accessories (Simple, Powered) · Class II · 21 CFR 882.4310
HWE — Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment · Class I · 21 CFR 878.4820
UDILibrary device dossier · generated 2026-09-11 · 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
2.6
2019-02
0
3.59
2019-03
0
3.95
2019-04
0
3.38
2019-05
0
3.72
2019-06
0
3.6
2019-07
0
3.12
2019-08
0
4.2
2019-09
0
3.57
2019-10
0
3.61
2019-11
0
4.18
2019-12
0
4.78
2020-01
0
3.71
2020-02
0
4.11
2020-03
0
5.18
2020-04
0
3.08
2020-05
0
3.01
2020-06
0
3.69
2020-07
0
3.49
2020-08
0
3.41
2020-09
0
4.23
2020-10
0
3.8
2020-11
0
3.97
2020-12
0
4.02
2021-01
0
3.21
2021-02
0
3.73
2021-03
0
3.71
2021-04
0
3.14
2021-05
0
3.48
2021-06
0
3.41
2021-07
0
3.24
2021-08
0
3.63
2021-09
0
3.29
2021-10
0
2.74
2021-11
0
3.15
2021-12
0
3.24
2022-01
0
2.88
2022-02
0
3.24
2022-03
0
3.62
2022-04
0
2.71
2022-05
0
3.27
2022-06
0
3.84
2022-07
0
2.86
2022-08
0
3.38
2022-09
0
4.15
2022-10
0
3.45
2022-11
0
3.77
2022-12
0
4.11
2023-01
0
2.95
2023-02
0
3.42
2023-03
0
3.4
2023-04
0
2.74
2023-05
0
3.98
2023-06
0
3.63
2023-07
0
2.98
2023-08
0
3.43
2023-09
0
3.59
2023-10
0
3.16
2023-11
0
4.98
2023-12
0
4.51
2024-01
0
3.32
2024-02
0
4.44
2024-03
0
4.56
2024-04
0
4.25
2024-05
0
5.29
2024-06
0
5.06
2024-07
0
4.14
2024-08
0
5.5
2024-09
0
7.47
2024-10
0
5
2024-11
0
5.9
2024-12
0
5.27
2025-01
0
3.75
2025-02
0
5.92
2025-03
0
6.61
2025-04
0
3.62
2025-05
0
4.66
2025-06
0
5.33
2025-07
0
4.7
2025-08
0
4.59
2025-09
0
4.77
2025-10
0
4.76
2025-11
0
6.48
2025-12
0
6.2
2026-01
0
3.77
2026-02
0
4.74
2026-03
0
5.51
2026-04
0
5.51
2026-05
0
6.09
2026-06
0
11.11
This device (reports/month)Average device in GWF, HBE, HWE (reports/device/month)
Regulatory clearances
K123270 SESE 2013-01-11 (k number procode)
Predicate lineage
K123270 — cited as predicate by K150796, K153463, K153587, K173338, K181111, K201407, K214011
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