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2.7mm Trephine Removal
Model 6008 · INTERVENTIONAL SPINE, INC · DI 00811954012694
HWK — Trephine · Class I · 21 CFR 888.4540
UDILibrary device dossier · generated 2026-09-12 · 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
2019-02
0
4
2019-03
0
1
2019-04
0
1
2019-07
0
1
2019-09
0
1
2019-10
0
1
2020-02
0
1
2020-03
0
1
2020-06
0
1
2020-07
0
1
2020-11
0
2
2020-12
0
1.5
2021-01
0
1
2021-02
0
2
2021-04
0
2
2021-07
0
1
2021-09
0
1
2021-11
0
1
2021-12
0
2
2022-02
0
1
2022-05
0
1
2022-06
0
1
2022-09
0
2
2022-10
0
2
2022-11
0
2
2023-02
0
2
2023-04
0
1.5
2023-06
0
2.5
2023-07
0
1
2023-10
0
1
2023-12
0
2
2024-02
0
1
2024-06
0
1
2024-10
0
2
2024-11
0
1
2025-03
0
1
2025-05
0
1
2025-07
0
1
2025-12
0
1
2026-06
0
1
This device (reports/month)Average device in HWK (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Manufacturer compliance record — INTERVENTIONAL SPINE, INC
NAI 2011-10-14 Interventional Spine Inc · 0 citations