510(k) · Cleared

Cleared

Ace Universal Reconstruction Plate

K930592510(k) TraditionalCleared Jul 26, 1993172-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

Ace Medical Co. · HRS Plate, Fixation, Bone

Cleared on Jul 26, 1993 after a 172-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 11 later devices descend from it.

Decided: Jul 26, 1993
Review: 172 days
Class: Class II
Product code: HRS
Recalls: None
Predicates: 0

11 later devices descend from it, 2 citing it directly.

This deviceK930592 Ace Universal Reconstruction PlateAce Medical Co. · 1993
Descendant · cites it directly · 8 of its ownK972219 Orthopedic Plate SystemFerguson Medical · 1997
Descendant · 2 generations on · 7 of its ownK022139 Hip Tool ImplantOrthopedic Sciences, Inc. · 2002
Descendant · cites it directly · 1 of its ownK111663 Trauma Internal Fixation SystemsDePuy Orthopaedics, Inc. · 2012 · Recalled
Descendant · 3 generations on · 1 of its ownK063709 TS-Bone Hip ToolOrthopedic Sciences, Inc. · 2007
Descendant · 3 generations on · 1 of its ownK040850 Tsy Shoulder Plate ImplantOrthopedic Sciences, Inc. · 2004

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

1997high 3 (2005) · low 0 (1998)2026

Most influential descendants

Showing 5 of 11 · See all

K972219Orthopedic Plate SystemFerguson Medical · 1997 · cites it directly8descendants
K022139Hip Tool ImplantOrthopedic Sciences, Inc. · 2002 · 2 generations on7descendants
K111663Trauma Internal Fixation SystemsDePuy Orthopaedics, Inc. · 2012 · cites it directly1descendant
K063709TS-Bone Hip ToolOrthopedic Sciences, Inc. · 2007 · 3 generations on1descendant
K040850Tsy Shoulder Plate ImplantOrthopedic Sciences, Inc. · 2004 · 3 generations on1descendant

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K930592	Ace Universal Reconstruction Plate	Ace Medical Co.	1993	—
+1	K972219	Orthopedic Plate System	Ferguson Medical	1997	—
+2	K022139	Hip Tool Implant	Orthopedic Sciences, Inc.	2002	—
+1	K111663	Trauma Internal Fixation Systems	DePuy Orthopaedics, Inc.	2012	17
+3	K063709	TS-Bone Hip Tool	Orthopedic Sciences, Inc.	2007	—
+3	K040850	Tsy Shoulder Plate Implant	Orthopedic Sciences, Inc.	2004	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
1997	1	0
2002	1	0
2004	1	0
2005	3	0
2006	1	0
2007	2	0
2012	1	0
2025	1	0

FIG. 1 — Lineage of K930592, 1993–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), 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

Get a 510(k) Report

What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (11)

See all 11

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K972219	Orthopedic Plate System	Ferguson Medical	1997	8
K111663	Trauma Internal Fixation Systems	DePuy Orthopaedics, Inc.	2012	1

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?

Of its descendants, K972219 (Ferguson Medical, 1997) has gone furthest, with 8 descendants of its own.

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	—

https://510kreport.com/device/K930592 · printed Nov 3, 2026

Cite this page

510(k) Report. “K930592: Ace Universal Reconstruction Plate.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K930592

Report an extraction error

Are you the manufacturer?

Record history

FDA decision record loaded May 2, 2026
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026