510(k) · Cleared

Cleared

Trochanter Cable Grip System (Add'l Indications)

K900926510(k) TraditionalCleared Apr 23, 199055-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

Cleared on Apr 23, 1990 after a 55-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 46 later devices descend from it.

Decided: Apr 23, 1990
Review: 55 days
Class: Class II
Product code: LRN
Recalls: None
Predicates: 0

46 later devices descend from it, 9 citing it directly.

This deviceK900926 Trochanter Cable Grip System (Add'l Indications)Howmedica Corp. · 1990
Descendant · cites it directly · 33 of its ownK961569 Dall-Miles Stainless Steel Beaded CableHowmedica Corp. · 1996
Descendant · cites it directly · 28 of its ownK971741 Dall-Miles Homogeneous Stainless Steel Cable and Beaded CableHowmedica Corp. · 1997
Descendant · 2 generations on · 17 of its ownK982545 BMP Cable SystemBiomet, Inc. · 1998 · Recalled
Descendant · 2 generations on · 10 of its ownK031162 Smith & Nephew Orthopaedic Cabling SystemSmith & Nephew, Inc. · 2003
Descendant · cites it directly · 10 of its ownK992616 SDB Cerclage SystemPioneer Surgical Technology · 1999

Showing 5 of 46 descendants. See all descendants

Descendants cleared per year

1996high 5 (2023) · low 0 (2000)2026

Most influential descendants

Showing 5 of 46 · See all

K961569Dall-Miles Stainless Steel Beaded CableHowmedica Corp. · 1996 · cites it directly33descendants
K971741Dall-Miles Homogeneous Stainless Steel Cable and Beaded CableHowmedica Corp. · 1997 · cites it directly28descendants
K982545BMP Cable SystemBiomet, Inc. · 1998 · 2 generations on17descendants
K031162Smith & Nephew Orthopaedic Cabling SystemSmith & Nephew, Inc. · 2003 · 2 generations on10descendants
K992616SDB Cerclage SystemPioneer Surgical Technology · 1999 · cites it directly10descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K900926	Trochanter Cable Grip System (Add'l Indications)	Howmedica Corp.	1990	—
+1	K961569	Dall-Miles Stainless Steel Beaded Cable	Howmedica Corp.	1996	—
+1	K971741	Dall-Miles Homogeneous Stainless Steel Cable and Beaded Cable	Howmedica Corp.	1997	—
+2	K982545	BMP Cable System	Biomet, Inc.	1998	1
+2	K031162	Smith & Nephew Orthopaedic Cabling System	Smith & Nephew, Inc.	2003	—
+1	K992616	SDB Cerclage System	Pioneer Surgical Technology	1999	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
1996	2	0
1997	2	0
1998	3	0
1999	2	0
2001	1	0
2003	3	0
2005	1	0
2006	1	0
2007	2	0
2009	1	0
2010	1	0
2013	1	0
2014	3	0
2015	2	0
2016	1	0
2018	1	0
2020	2	0
2021	2	0
2022	1	0
2023	5	0
2024	3	0
2025	3	0
2026	3	0

FIG. 1 — Lineage of K900926, 1990–2026Source: 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 LRN? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Candidate predicates for a device like this, rankedin the report
Recall history across each candidate’s familyin the report

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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (46)

See all 46

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

Number	Device	Applicant	Decided	Descendants
K961569	Dall-Miles Stainless Steel Beaded Cable	Howmedica Corp.	1996	33
K971741	Dall-Miles Homogeneous Stainless Steel Cable and Beaded Cable	Howmedica Corp.	1997	28
K992616	SDB Cerclage System	Pioneer Surgical Technology	1999	10
K962162	Dall-Miles Trochanter Cable Supergrip	Howmedica Corp.	1996	10
K202016	Dall-Miles® Cable System	Howmedica Osteonics Corp., Dba Stryker Orthopaedics	2020	8
K972327	Metagen Activelock Cerclage System	Pacific Materials and Interfaces	1997	3
K984432	Dall-Miles Cable Grip (a-Grip)	Howmedica Osteonics Corp.	1999	2
K983976	Metagen Activelock Wire Cerclage System	Metagen, LLC	1998	2
K981631	Influence Clip System	Influence, Inc.	1998	0

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, K961569 (Howmedica Corp., 1996) has gone furthest, with 33 descendants of its own.

How does its category compare?

All LRN devices

LRN Wire, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LRN

FDA has decided no LRN device since 2007.

Median 510(k) review, days · LRN

Too few LRN 510(k)s in any year since 2007 to give a median.

Recalls per year · LRN

1in 2019

2007high 1 (2019) · low 0 (2007)2026

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

Adverse event reports per year · LRN

81in 2025

2007high 140 (2023) · low 3 (2007)2025

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

View these four charts as a table

Year	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	—	0	3
2008	—	0	20
2009	—	0	31
2010	—	0	13
2011	—	0	6
2012	—	0	25
2013	—	0	108
2014	—	0	57
2015	—	0	24
2016	—	0	38
2017	—	0	33
2018	—	0	58
2019	—	1	84
2020	—	0	68
2021	—	0	118
2022	—	0	106
2023	—	0	140
2024	—	0	87
2025	—	0	81
2026	—	0	—

https://510kreport.com/device/K900926 · printed Nov 6, 2026

Cite this page

510(k) Report. “K900926: Trochanter Cable Grip System (Add'l Indications).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K900926

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Record history

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