510(k) Report

510(k) · Cleared

Cleared

Trochanter Cable Grip System

K844068510(k) TraditionalCleared Jun 21, 1985246-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

Howmedica Corp. · KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Cleared on Jun 21, 1985 after a 246-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 43 later devices descend from it.

Decided
Jun 21, 1985
Review
246 days
Class
Class II
Product code
KTT
Recalls
None
Predicates
0

43 later devices descend from it, 6 citing it directly.

Descendants, by year cleared 1996: 1 descendant cleared1999: 2 descendants cleared1998: 2 descendants cleared1997: 2 descendants cleared2003: 3 descendants cleared2020: 2 descendants cleared2006: 1 descendant cleared2005: 1 descendant cleared2023: 5 descendants cleared2015: 2 descendants cleared2021: 2 descendants cleared2010: 1 descendant cleared2013: 1 descendant cleared2018: 1 descendant cleared2024: 3 descendants cleared2009: 1 descendant cleared2014: 3 descendants cleared2016: 1 descendant cleared2026: 3 descendants cleared2001: 1 descendant cleared2007: 1 descendant cleared2022: 1 descendant cleared2025: 3 descendants cleared1990200020102020
  1. This deviceK844068 Trochanter Cable Grip SystemHowmedica Corp. · 1985
  2. Descendant · cites it directly · 33 of its ownK961569 Dall-Miles Stainless Steel Beaded CableHowmedica Corp. · 1996
  3. Descendant · cites it directly · 28 of its ownK971741 Dall-Miles Homogeneous Stainless Steel Cable and Beaded CableHowmedica Corp. · 1997
  4. Descendant · 2 generations on · 17 of its ownK982545 BMP Cable SystemBiomet, Inc. · 1998 · Recalled
  5. Descendant · 2 generations on · 10 of its ownK031162 Smith & Nephew Orthopaedic Cabling SystemSmith & Nephew, Inc. · 2003
  6. Descendant · cites it directly · 10 of its ownK992616 SDB Cerclage SystemPioneer Surgical Technology · 1999

Showing 5 of 43 descendants. See all descendants

Descendants cleared per year

1996: 11997: 21998: 21999: 22001: 12003: 32005: 12006: 12007: 12009: 12010: 12013: 12014: 32015: 22016: 12018: 12020: 22021: 22022: 12023: 52024: 32025: 32026: 3
1996high 5 (2023) · low 0 (2000)2026

Most influential descendants

Showing 5 of 43 · 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

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K844068Trochanter Cable Grip SystemHowmedica Corp.1985—
+1K961569Dall-Miles Stainless Steel Beaded CableHowmedica Corp.1996—
+1K971741Dall-Miles Homogeneous Stainless Steel Cable and Beaded CableHowmedica Corp.1997—
+2K982545BMP Cable SystemBiomet, Inc.19981
+2K031162Smith & Nephew Orthopaedic Cabling SystemSmith & Nephew, Inc.2003—
+1K992616SDB Cerclage SystemPioneer Surgical Technology1999—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199720
199820
199920
200110
200330
200510
200610
200710
200910
201010
201310
201430
201520
201610
201810
202020
202120
202210
202350
202430
202530
202630
FIG. 1 — Lineage of K844068, 1985–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

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 KTT? 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 KTT device

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  2. #2 Held for the reportin 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? (43)

See all 43

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

NumberDeviceApplicantDecidedDescendants
K961569Dall-Miles Stainless Steel Beaded CableHowmedica Corp.199633
K971741Dall-Miles Homogeneous Stainless Steel Cable and Beaded CableHowmedica Corp.199728
K992616SDB Cerclage SystemPioneer Surgical Technology199910
K972327Metagen Activelock Cerclage SystemPacific Materials and Interfaces19973
K984432Dall-Miles Cable Grip (a-Grip)Howmedica Osteonics Corp.19992
K983976Metagen Activelock Wire Cerclage SystemMetagen, LLC19982

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 KTT devices

KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KTT

10in 2025

2007: 92008: 112009: 112010: 122011: 102012: 92013: 72014: 142015: 122016: 102017: 112018: 62019: 82020: 92021: 102022: 32023: 72024: 52025: 102026 (partial year): 5
2007high 14 (2014) · low 3 (2022)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KTT

88in 2025

2007: 55 days median2008: 73 days median2009: 94 days median2010: 148 days median2011: 157 days median2012: 140 days median2013: 87 days median2014: 129 days median2015: 60 days median2016: 142 days median2017: 184 days median2018: 149 days median2019: 110 days median2020: 200 days median2021: 83 days median2022: 25 days median2023: 29 days median2024: 90 days median2025: 88 days median2026 (partial year): 68 days median
2007high 200 (2020) · low 25 (2022)2026

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

Recalls per year · KTT

2in 2021

2007: 22008: 12009: 22010: 12012: 42013: 72017: 12018: 142019: 32021: 22026 (partial year): 11
2007high 14 (2018) · low 0 (2011)2026

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

Adverse event reports per year · KTT

673in 2025

2007: 452008: 662009: 452010: 1212011: 1962012: 5272013: 8982014: 4452015: 4012016: 4002017: 4852018: 5972019: 8002020: 9422021: 9612022: 6272023: 5542024: 5232025: 673
2007high 961 (2021) · low 45 (2007)2025

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

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007955245
20081173166
20091194245
2010121481121
2011101570196
201291404527
20137877898
2014141290445
201512600401
2016101420400
2017111841485
2018614914597
201981103800
202092000942
202110832961
20223250627
20237290554
20245900523
202510880673
202656811—
Cite this page

510(k) Report. “K844068: Trochanter Cable Grip System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K844068

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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