510(k) · Cleared

Cleared

Solco 4CIS General Plate System

K051155510(k) TraditionalCleared Jul 11, 200568-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

Solco Biomedical Co., Ltd. · HRS Plate, Fixation, Bone

Cleared on Jul 11, 2005 as substantially equivalent to K042377 (Synthes (Usa), 2004) and 1 other predicate after a 68-day review. Its family tree reaches back 1 generation to 1999.

Decided: Jul 11, 2005
Review: 68 days
Class: Class II
Product code: HRS
Recalls: None
Predicates: 2

Its longest line of descent runs back 1 generation to K993106 (1999). 2 ancestors in all. No later device cites it as a predicate yet.

By dateBy generation

Root · 1 generation backK993106 Smith & Nephew Bone Plate System (Bone Plates, Bone Screws and…Smith & Nephew, Inc. · 1999
This deviceK051155 Solco 4CIS General Plate SystemSolco Biomedical Co., Ltd. · 2005

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K993106	Smith & Nephew Bone Plate System (Bone Plates, Bone Screws and Accessories)	Smith & Nephew, Inc.	1999	—
0 (this device)	K051155	Solco 4CIS General Plate System	Solco Biomedical Co., Ltd.	2005	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
2004	1	0

FIG. 1 — Lineage of K051155, 1999–2005Source: 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? (2)

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
*	K042377	Synthes Low Profile Reconstruction Plates Summary page 1 …used to equivalent in function, design, composition. material and intended 1) Synthes Low Profile Reconstruction Plates (K042377) and 2) Smith & Nephew Bone Plate System (K993 106). Device Description…	Synthes (Usa)	2004	—
*	K993106	Smith & Nephew Bone Plate System (Bone Plates, Bone Screws and Accessories) Summary page 1 …n function, design, composition. material and intended 1) Synthes Low Profile Reconstruction Plates (K042377) and 2) Smith & Nephew Bone Plate System (K993 106). Device Description Tubular plate, Th…	Smith & Nephew, Inc.	1999	—

Also cleared against K042377: 5 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?

None of the 2 ancestors has a recall.
5 other devices also cite its predicate K042377.

How does its category compare?

All HRS devices

HRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years.

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 SOLCO 4CIS® General Plate System is used for adult or pediatric patients as indicated for pelvic, small, and long bone fracture fixation. Indications for use include fractures of the tibia, fibula, femur, pelvis, metacarpals, metatarsals, humerus, ulna, radius, hand and middle foot bones.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K051155 · printed Nov 6, 2026

Cite this page

510(k) Report. “K051155: Solco 4CIS General Plate System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K051155

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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