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Vu ePOD™
Model 14-LT-2216 · Seaspine Orthopedics Corporation · DI 10889981038908
MAX — Intervertebral Fusion Device With Bone Graft, Lumbar · Class II · 21 CFR 888.3080
MQP — Spinal Vertebral Body Replacement Device · Class II · 21 CFR 888.3060
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
1.59
2019-02
0
1.26
2019-03
0
1.76
2019-04
0
1.41
2019-05
0
1.59
2019-06
0
1.67
2019-07
0
1.59
2019-08
0
1.4
2019-09
0
1.3
2019-10
0
1.77
2019-11
0
1.52
2019-12
0
1.44
2020-01
0
1.65
2020-02
0
1.63
2020-03
0
1.45
2020-04
0
1.39
2020-05
0
1.5
2020-06
0
1.74
2020-07
0
2
2020-08
0
1.58
2020-09
0
2.26
2020-10
0
1.9
2020-11
0
1.76
2020-12
0
1.65
2021-01
0
1.56
2021-02
0
1.58
2021-03
0
1.92
2021-04
0
1.52
2021-05
0
1.48
2021-06
0
2.39
2021-07
0
1.68
2021-08
0
2
2021-09
0
1.66
2021-10
0
2
2021-11
0
1.77
2021-12
0
2.15
2022-01
0
2.59
2022-02
0
2.21
2022-03
0
1.74
2022-04
0
1.73
2022-05
0
2.04
2022-06
0
1.76
2022-07
0
1.96
2022-08
0
1.76
2022-09
0
1.88
2022-10
0
1.7
2022-11
0
1.91
2022-12
0
1.62
2023-01
0
2.39
2023-02
0
1.94
2023-03
0
1.95
2023-04
0
1.71
2023-05
0
1.79
2023-06
0
1.68
2023-07
0
2.03
2023-08
0
1.71
2023-09
0
1.89
2023-10
0
1.81
2023-11
0
8.19
2023-12
0
3.09
2024-01
0
1.85
2024-02
0
2.05
2024-03
0
1.92
2024-04
0
1.41
2024-05
0
1.7
2024-06
0
1.73
2024-07
0
1.84
2024-08
0
1.87
2024-09
0
1.83
2024-10
0
1.93
2024-11
0
1.67
2024-12
0
1.63
2025-01
0
1.73
2025-02
0
1.68
2025-03
0
2.02
2025-04
0
1.61
2025-05
0
1.88
2025-06
0
1.91
2025-07
0
1.72
2025-08
0
1.63
2025-09
0
1.58
2025-10
0
1.68
2025-11
0
1.87
2025-12
0
1.78
2026-01
0
1.78
2026-02
0
1.47
2026-03
0
2.45
2026-04
0
1.65
2026-05
0
1.6
2026-06
0
1.63
This device (reports/month)Average device in MAX, MQP (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Predicate lineage
K082712 — cited as predicate by K111965, K142488, K173260
Lineage extracted from public 510(k) summary text (heuristic).
Manufacturer compliance record — Seaspine Orthopedics Corporation
Warning Letter 2026-02-24 IsoTis OrthoBiologics, Inc.
OAI 2025-10-17 IsoTis OrthoBiologics, Inc. · 3 citations
NAI 2022-04-22 SEASPINE ORTHOPEDICS CORPORATION · 0 citations
NAI 2022-04-22 SEASPINE ORTHOPEDICS CORPORATION · 0 citations
NAI 2018-08-14 SEASPINE ORTHOPEDICS CORPORATION · 0 citations
NAI 2018-08-14 SEASPINE ORTHOPEDICS CORPORATION · 0 citations
NAI 2015-09-25 IsoTis OrthoBiologics, Inc. · 0 citations
NAI 2012-04-27 IsoTis OrthoBiologics, Inc. · 0 citations