510(k) · Cleared

Cleared

Arthrex Mini Comprehensive Fixation System – 1.4mm & 1.6mm Module

K191326510(k) TraditionalCleared Oct 15, 2019152-day reviewClass II21 CFR 888.3030

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Arthrex, Inc. · HRS Plate, Fixation, Bone

Cleared on Oct 15, 2019 as substantially equivalent to K030310 (Synthes (Usa), 2003) after a 152-day review. Its family tree reaches back 1 generation to 2003.

Decided: Oct 15, 2019
Review: 152 days
Class: Class II
Product code: HRS
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K030310 (2003). No later device cites it as a predicate yet.

By dateBy generation

Root · 1 generation backK030310 Synthes Stainless Steel Modular Hand SystemSynthes (Usa) · 2003
This deviceK191326 Arthrex Mini Comprehensive Fixation System – 1.4mm & 1.6mm ModuleArthrex, Inc. · 2019

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K030310	Synthes Stainless Steel Modular Hand System	Synthes (Usa)	2003	—
0 (this device)	K191326	Arthrex Mini Comprehensive Fixation System – 1.4mm & 1.6mm Module	Arthrex, Inc.	2019	—

FIG. 1 — Lineage of K191326, 2003–2019Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in HRS? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new HRS device

#1 K222465 Tyber Medical Anatomical Plating Systemscore 27.5 · 16 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

Type	Number	Device	Applicant	Decided	Recalls
*	K030310	Synthes Stainless Steel Modular Hand System Summary page 4 …and accessories 21 CFR 888.3040: Smooth or threaded metallic bone fixation fastener Regulatory Class II Predicate Device K030310: Synthes Stainless Steel Modular Hand System Purpose of This Traditional 510(k) premarket notification is submitted to…	Synthes (Usa)	2003	—

Also cleared against K030310: 15 other devices →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

Its one ancestor has no recall.
15 other devices also cite its predicate K030310.

How does its category compare?

All HRS devices

HRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · HRS

54in 2025

2007high 76 (2014) · low 35 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HRS

90in 2025

2007high 144 (2022) · low 57 (2014)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · HRS

1in 2025

2007high 25 (2019) · low 0 (2014)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · HRS

2,306in 2025

2007high 3,359 (2019) · low 311 (2008)2025

MAUDE reports naming product code HRS, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	35	63	2	339
2008	35	87	11	311
2009	47	85	3	435
2010	49	100	16	491
2011	43	88	5	773
2012	59	106	4	1,663
2013	56	89	11	2,643
2014	76	57	0	2,413
2015	56	97	7	3,095
2016	44	109	5	2,276
2017	57	122	3	2,220
2018	40	116	2	2,663
2019	46	89	25	3,359
2020	48	88	1	2,790
2021	40	87	9	2,442
2022	47	144	3	1,700
2023	40	120	1	2,049
2024	54	96	0	1,849
2025	54	90	1	2,306
2026	51	82	3	—

What is it indicated for?

The Arthrex Mini Comprehensive Fixation System Plates (1.4-1.6 mm) are intended for use in selective trauma, reconstructive procedures, and general surgery of the hand, wrist, and other small bones. The Arthrex Comprehensive Fixation System Plates are to be used with the Arthrex Mini Comprehensive Fixation System Screws (1.4-1.6 mm solid).

The Arthrex Mini Comprehensive Fixation System Screws (1.4-1.6 mm solid) are intended for use in selective trauma, reconstructive procedures, and general surgery of the hand, wrist, and other small bones. The Arthrex Comprehensive Fixation System Screws are to be used with the Arthrex Mini Comprehensive Fixation System Plates (1.4-1.6 mm).

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K191326 · printed Nov 6, 2026

Cite this page

510(k) Report. “K191326: Arthrex Mini Comprehensive Fixation System – 1.4mm & 1.6mm Module.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K191326

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Record history

FDA decision record loaded May 2, 2026
Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026