510(k) Report

510(k) · Cleared

Cleared

Dall-Miles Trochanter Cable Supergrip

K962162510(k) TraditionalCleared Aug 14, 199671-day reviewClass II21 CFR 888.3010

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

Howmedica Corp. · JDQ Cerclage, Fixation

Cleared on Aug 14, 1996 as substantially equivalent to K872224 (Howmedica Corp., 1987) and 1 other predicate after a 71-day review. Its family tree reaches back 1 generation to 1987. 10 later devices descend from it.

Decided
Aug 14, 1996
Review
71 days
Class
Class II
Product code
JDQ
Recalls
None
Predicates
2

Its longest line of descent runs back 1 generation to K872224 (1987). 2 ancestors in all. 10 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1990: 1 other ancestor2007: 1 descendant cleared2020: 1 descendant cleared2024: 2 descendants cleared2023: 2 descendants cleared2026: 2 descendants cleared2025: 2 descendants clearedK872224 · Modified Trochanter Cable Grip System · Howmedica Corp. · 1987 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant3 generations forward: 4 descendants4 generations forward: 4 descendants K872224 · Modified Trochanter Cable Grip System · Howmedica Corp. · 1987 · recalled0
  1. Root · 1 generation backK872224 Modified Trochanter Cable Grip SystemHowmedica Corp. · 1987 · Recalled
  2. This deviceK962162 Dall-Miles Trochanter Cable SupergripHowmedica Corp. · 1996
  3. Descendant · cites it directly · 9 of its ownK070170 Dall-Miles SystemStryker Orthopaedics · 2007
  4. Descendant · 2 generations on · 8 of its ownK202016 Dall-Miles® Cable SystemHowmedica Osteonics Corp., Dba Stryker Orthopaedics · 2020
  5. Descendant · 3 generations on · 4 of its ownK233498 Stryker Orthopaedics Hip Systems Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics · 2023
  6. Descendant · 4 generations on · 2 of its ownK243784 Stryker Orthopaedics Hip Devices Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics · 2025
  7. Descendant · 3 generations on · 1 of its ownK231257 Pangea Utility Plating System, Pangea PlatformStryker GmbH · 2023

Showing 5 of 10 descendants. See all descendants

Descendants cleared per year

2007: 12020: 12023: 22024: 22025: 22026: 2
2007high 2 (2023) · low 0 (2008)2026

Most influential descendants

Showing 5 of 10 · See all
  • K070170Dall-Miles SystemStryker Orthopaedics · 2007 · cites it directly9descendants
  • K202016Dall-Miles® Cable SystemHowmedica Osteonics Corp., Dba Stryker Orthopaedics · 2020 · 2 generations on8descendants
  • K233498Stryker Orthopaedics Hip Systems Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics · 2023 · 3 generations on4descendants
  • K243784Stryker Orthopaedics Hip Devices Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics · 2025 · 4 generations on2descendants
  • K231257Pangea Utility Plating System, Pangea PlatformStryker GmbH · 2023 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K872224Modified Trochanter Cable Grip SystemHowmedica Corp.19872
0 (this device)K962162Dall-Miles Trochanter Cable SupergripHowmedica Corp.1996—
+1K070170Dall-Miles SystemStryker Orthopaedics2007—
+2K202016Dall-Miles® Cable SystemHowmedica Osteonics Corp., Dba Stryker Orthopaedics2020—
+3K233498Stryker Orthopaedics Hip Systems Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics2023—
+4K243784Stryker Orthopaedics Hip Devices Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics2025—
+3K231257Pangea Utility Plating System, Pangea PlatformStryker GmbH2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
202010
202320
202420
202520
202620
FIG. 1 — Lineage of K962162, 1987–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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

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 JDQ? 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 JDQ device

  1. #1 K261271 Cable-Ready® Cable Grip Systemscore 14.7 · 11 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (3)

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.

TypeNumberDeviceApplicantDecidedRecalls
*K872224Modified Trochanter Cable Grip System
Summary page 1
…6870 Date Summary Prepared: 6/3/96 The Dall-Miles Trochanter Cable Grip described in this submission is a modification of the original Dall-Miles Cable Grip cleared in (K 872224). The Grip component provides for trochanteric reattachment following osteotomy in Total Hip Arthroplasty. The proximal hooks of…
Howmedica Corp.19872
*K900926Trochanter Cable Grip System (Add'l Indications)
Summary page 1
…nce in intended use, materials, design, operational principles, and indications and contraindications to Howmedica's original Dall-Miles Cable Grip System (K 872224 and K 900926) and Biomet Medical Products' BMP Cable Systen.
Howmedica Corp.1990—
*—BMP Cable System
Named without a submission number
—

Also cleared against K872224: 1 other device →

What descends from it? (10)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K070170Dall-Miles SystemStryker Orthopaedics20079

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?

  • 1 of the 2 ancestors has a recall of any class.
  • Of its descendants, K070170 (Stryker Orthopaedics, 2007) has gone furthest, with 9 descendants of its own.
  • 1 other device also cites its predicate K872224.

How does its category compare?

All JDQ devices

JDQ Cerclage, Fixation: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JDQ

2in 2025

2007: 12008: 22009: 22011: 62012: 32013: 12014: 22015: 52016: 42017: 12018: 62020: 42022: 22023: 32024: 32025: 22026 (partial year): 1
2007high 6 (2011) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JDQ

130in 2024

2011: 130 days median2012: 134 days median2015: 92 days median2016: 129 days median2018: 101 days median2020: 93 days median2023: 141 days median2024: 130 days median
2007high 141 (2023) · low 92 (2015)2026

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

Recalls per year · JDQ

5in 2019

2008: 22010: 22013: 12015: 12019: 5
2007high 5 (2019) · low 0 (2007)2026

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

Adverse event reports per year · JDQ

84in 2025

2007: 52008: 252009: 192010: 282011: 302012: 1302013: 3212014: 2232015: 2052016: 2242017: 1382018: 1822019: 1582020: 1252021: 1412022: 1342023: 982024: 1152025: 84
2007high 321 (2013) · low 5 (2007)2025

MAUDE reports naming product code JDQ, 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
20071—05
20082—225
20092—019
20100—228
20116130030
201231340130
20131—1321
20142—0223
20155921205
201641290224
20171—0138
201861010182
20190—5158
20204930125
20210—0141
20222—0134
20233141098
202431300115
20252—084
20261—0—

Also cleared against K872224

1 other device cites the same predicate.

  • K992616SDB Cerclage SystemPioneer Surgical Technology · 1999

More from Howmedica Corp.

393 FDA decisions under this applicant name. See the company

  • N17004/S013Surgical Simplex P Bone CementHowmedica Corp. · 2000
  • N17004/S012Surgical Simplex P Radiopaque Bone CementHowmedica Corp. · 2000
  • K983528Micro Dynamic MeshHowmedica Corp. · 1998
  • K983404Type 3 Femoral ComponentsHowmedica Corp. · 19981 recall
  • K980925Duration II Tibial Inserts-Ethylene Oxide SterilizationHowmedica Corp. · 1998

Recent decisions in JDQ

The JDQ category page

  • K261271Cable-Ready® Cable Grip SystemPioneer Surgical Technology, Inc. · 2026
  • K243905Stitch Cerclage – Suture TapesGM Dos Reis Industria e Comercio Ltda. · 2025
  • K243344Arthrex FiberTape and TigerTape Cerclage Sutures; Arthrex Radiopaque FiberTape Cerclage SuturesArthrex, Inc. · 2025
  • K232733Mbrace CableMedacta International S.A. · 2024
  • K233949ACCORD Cable SystemSmith & Nephew, Inc. · 2024

https://510kreport.com/device/K962162 · printed Nov 4, 2026

Cite this page

510(k) Report. “K962162: Dall-Miles Trochanter Cable Supergrip.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K962162

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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