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Unnamed device
Model 6002-350-000 · Stryker Leibinger GmbH & Co. KG · DI 04546540503824
HAW — Neurological Stereotaxic Instrument · Class II · 21 CFR 882.4560
UDILibrary device dossier · generated 2026-09-16 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (1)
Initiated
Recall #
Class
Status
Reason
Link basis
2017-10-16
Z-1216-2018
Class II
Terminated
Stryker Instruments and Stryker Leibinger GmbH & Co. KG are
voluntarily recalling certain serial numbers Thoracic Pedicle Feelers that are used in conjunction with the Stryker Navigation
System because the settings on
the machine were higher than intended. This change led to increased energy directed onto the tip of the Thoracic Pedicle
Feeler which caused material degradation where the laser marks exist. There is the potential for the tip of the Thoracic Pedicle Feeler to break.
code info di
Adverse-event reports — MAUDE (33)
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.
Malfunction: 33
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-01
1
12.92
2019-02
0
14.35
2019-03
1
14.05
2019-04
0
18.63
2019-05
2
19.54
2019-06
2
20.19
2019-07
4
13.37
2019-08
0
11.15
2019-09
0
11.95
2019-10
2
9.58
2019-11
0
11.88
2019-12
1
14.46
2020-01
0
11.27
2020-02
0
12.22
2020-03
0
12.88
2020-04
0
10.44
2020-05
0
15.5
2020-06
0
12.21
2020-07
1
14.34
2020-08
0
12.98
2020-09
0
12.31
2020-10
1
12.61
2020-11
1
14.12
2020-12
0
12.64
2021-01
1
11.89
2021-02
0
14.14
2021-03
0
13.25
2021-04
0
13.21
2021-05
0
14.8
2021-06
0
18.26
2021-07
0
13.79
2021-08
0
17.29
2021-09
0
24.68
2021-10
0
14.32
2021-11
1
16.72
2021-12
0
12.67
2022-01
1
10.59
2022-02
0
13.53
2022-03
0
15.09
2022-04
0
12.75
2022-05
0
16.55
2022-06
0
15.68
2022-07
1
12.74
2022-08
0
13.73
2022-09
0
15.67
2022-10
0
18.18
2022-11
0
16.94
2022-12
1
16.56
2023-01
1
14
2023-02
0
12.62
2023-03
0
16.68
2023-04
1
14.38
2023-05
0
16.67
2023-06
0
24.22
2023-07
3
25.39
2023-08
1
21.23
2023-09
0
17.03
2023-10
1
17.29
2023-11
0
18.43
2023-12
2
20.54
2024-01
0
25.65
2024-02
0
20.49
2024-03
0
21.69
2024-04
0
22.32
2024-05
0
18.44
2024-06
0
19.81
2024-07
1
23.6
2024-08
0
29.73
2024-09
0
22.75
2024-10
1
27.4
2024-11
0
14.37
2024-12
1
16.74
2025-01
0
16.27
2025-02
0
21.38
2025-03
0
25.24
2025-04
0
23.34
2025-05
0
20.44
2025-06
0
33.41
2025-07
0
20.35
2025-08
0
17.63
2025-09
0
19.99
2025-10
0
18.6
2025-11
0
16.83
2025-12
0
15.93
2026-01
0
17
2026-02
0
14.12
2026-03
0
15.06
2026-04
0
11.52
2026-05
0
11.51
2026-06
0
8.95
This device (reports/month)Average device in HAW (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Manufacturer compliance record — Stryker Leibinger GmbH & Co. KG
NAI 2025-02-27 Stryker Leibinger GmbH & Co. KG · 0 citations
NAI 2017-07-27 Stryker Leibinger GmbH & Co. KG · 0 citations
NAI 2013-11-14 Stryker Leibinger GmbH & Co. KG · 0 citations