510(k) Report

510(k) · Cleared

Cleared

ES Trochanteric Nail, Left and Right, 10MM

K103533510(k) SpecialCleared Jan 19, 201149-day reviewClass II21 CFR 888.3020

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

Advanced Orthopaedic Solutions, Inc. · HSB Rod, Fixation, Intramedullary And Accessories

Cleared on Jan 19, 2011 as substantially equivalent to K021008 (Advanced Orthopaedic Solutions, Inc., 2002) after a 49-day review. Its family tree reaches back 4 generations to 1997. 11 later devices descend from it.

Decided
Jan 19, 2011
Review
49 days
Class
Class II
Product code
HSB
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K970097 (1997). 13 ancestors in all, the oldest K871539 (1987). 11 later devices descend from it, 6 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2001: 3 other ancestors1999: 1 other ancestor1995: 1 other ancestor1992: 1 other ancestor1991: 1 other ancestor1998: 1 other ancestor1987: 1 other ancestor2023: 1 descendant cleared2019: 1 descendant cleared2013: 1 descendant cleared2014: 1 descendant cleared2020: 1 descendant cleared2012: 1 descendant cleared2022: 1 descendant cleared2025: 2 descendants cleared2026: 1 descendant cleared2024: 1 descendant clearedK970097 · Proximal Femoral Nail (PFN) System · Synthes (Usa) · 1997K973240 · Synthes Proximal Femoral Nail (PFN) System Modification · Synthes (Usa) · 1997K013563 · Long Trochanteric Nail System · DePuy Orthopaedics, Inc. · 2001 · recalledK021008 · Advanced Orthopaedic Solutions Trochanteric Nail · Advanced Orthopaedic Solutions, Inc. · 2002 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 7 other ancestors3 generations back: 2 other ancestors 1 generation forward: 6 descendants2 generations forward: 4 descendants3 generations forward: 1 descendant K021008 · Advanced Orthopaedic Solutions Trochanteric Nail · Advanced Orthopaedic Solutions, Inc. · 2002 · recalledK013563 · Long Trochanteric Nail System · DePuy Orthopaedics, Inc. · 2001 · recalledK973240 · Synthes Proximal Femoral Nail (PFN) System Modification · Synthes (Usa) · 1997K970097 · Proximal Femoral Nail (PFN) System · Synthes (Usa) · 19970
  1. Root · 4 generations backK970097 Proximal Femoral Nail (PFN) SystemSynthes (Usa) · 1997
  2. 3 generations backK973240 Synthes Proximal Femoral Nail (PFN) System ModificationSynthes (Usa) · 1997
  3. 2 generations backK013563 Long Trochanteric Nail SystemDePuy Orthopaedics, Inc. · 2001 · Recalled
  4. 1 generation backK021008 Advanced Orthopaedic Solutions Trochanteric NailAdvanced Orthopaedic Solutions, Inc. · 2002 · Recalled
  5. This deviceK103533 ES Trochanteric Nail, Left and Right, 10MMAdvanced Orthopaedic Solutions, Inc. · 2011
  6. Descendant · cites it directly · 6 of its ownK120148 Aos Solid Locking Lag Screw, Aos Telescoping Lag ScrewAdvanced Orthopaedic Solutions, Inc. · 2012
  7. Descendant · cites it directly · 4 of its ownK202099 AOS Galileo™ Trochanteric Nail SystemAdvanced Orthopaedic Solutions, Inc. · 2020
  8. Descendant · cites it directly · 2 of its ownK140601 Flow-NailFlow-Fx, LLC · 2014
  9. Descendant · cites it directly · 2 of its ownK133081 Trochanteric Nails and ES Trochanteric Nails, Humeral Naisl, Tibial…Advanced Orthopaedic Solutions, Inc. · 2013
  10. Descendant · cites it directly · 1 of its ownK230257 Arthrex Intramedullary NailsArthrex, Inc. · 2023

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2012: 12013: 12014: 12019: 12020: 12022: 12023: 12024: 12025: 22026: 1
2012high 2 (2025) · low 0 (2015)2026

Most influential descendants

Showing 5 of 11 · See all
  • K120148Aos Solid Locking Lag Screw, Aos Telescoping Lag ScrewAdvanced Orthopaedic Solutions, Inc. · 2012 · cites it directly6descendants
  • K202099AOS Galileo™ Trochanteric Nail SystemAdvanced Orthopaedic Solutions, Inc. · 2020 · cites it directly4descendants
  • K140601Flow-NailFlow-Fx, LLC · 2014 · cites it directly2descendants
  • K133081Trochanteric Nails and ES Trochanteric Nails, Humeral Naisl, Tibial Nails, Antegrade…Advanced Orthopaedic Solutions, Inc. · 2013 · cites it directly2descendants
  • K230257Arthrex Intramedullary NailsArthrex, Inc. · 2023 · cites it directly1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K970097Proximal Femoral Nail (PFN) SystemSynthes (Usa)1997—
−3K973240Synthes Proximal Femoral Nail (PFN) System ModificationSynthes (Usa)1997—
−2K013563Long Trochanteric Nail SystemDePuy Orthopaedics, Inc.200154
−1K021008Advanced Orthopaedic Solutions Trochanteric NailAdvanced Orthopaedic Solutions, Inc.200212
0 (this device)K103533ES Trochanteric Nail, Left and Right, 10MMAdvanced Orthopaedic Solutions, Inc.2011—
+1K120148Aos Solid Locking Lag Screw, Aos Telescoping Lag ScrewAdvanced Orthopaedic Solutions, Inc.2012—
+1K202099AOS Galileo™ Trochanteric Nail SystemAdvanced Orthopaedic Solutions, Inc.2020—
+1K140601Flow-NailFlow-Fx, LLC2014—
+1K133081Trochanteric Nails and ES Trochanteric Nails, Humeral Naisl, Tibial Nails…Advanced Orthopaedic Solutions, Inc.2013—
+1K230257Arthrex Intramedullary NailsArthrex, Inc.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
199110
199210
199510
199810
199910
200130

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
201310
201410
201910
202010
202210
202310
202410
202520
202610
FIG. 1 — Lineage of K103533, 1997–2026Source: 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 HSB? 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 HSB device

  1. #1 K200869 Gamma3 Systemscore 19.8 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

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
*K021008Advanced Orthopaedic Solutions Trochanteric Nail
Summary page 1
…ION: Class 11,21 CFR 888.3020 Intramedullary Fixation Rod DEVICE CODE: HSB SUBSTANTIALLY EQUIVALENT DEVICE: AOIS Trochanteric Nail (K021008, Cleared June 20, 2002) DEVICE DESCRIPTION: The AOS ESTm Trochanteric Nail is a Titanium…
Advanced Orthopaedic Solutions, Inc.200212

Also cleared against K021008: 6 other devices →

What descends from it? (11)

See all 11

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

NumberDeviceApplicantDecidedDescendants
K120148Aos Solid Locking Lag Screw, Aos Telescoping Lag ScrewAdvanced Orthopaedic Solutions, Inc.20126
K202099AOS Galileo™ Trochanteric Nail SystemAdvanced Orthopaedic Solutions, Inc.20204
K140601Flow-NailFlow-Fx, LLC20142
K133081Trochanteric Nails and ES Trochanteric Nails, Humeral Naisl, Tibial Nails, Antegrade…Advanced Orthopaedic Solutions, Inc.20132
K230257Arthrex Intramedullary NailsArthrex, Inc.20231
K191598AOS ES Retrograde Femoral NailAdvanced Orthopaedic Solutions, Inc.20190

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?

  • The line of descent spans 14 years and passes through 3 companies; a new generation was cleared every 4.1 years on median.
  • 5 of the 13 ancestors have a recall of any class.
  • Of its descendants, K120148 (Advanced Orthopaedic Solutions, Inc., 2012) has gone furthest, with 6 descendants of its own.
  • 6 other devices also cite its predicate K021008.

How does its category compare?

All HSB devices

HSB Rod, Fixation, Intramedullary And Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · HSB

15in 2025

2007: 82008: 112009: 182010: 142011: 162012: 172013: 182014: 192015: 222016: 82017: 232018: 172019: 132020: 172021: 102022: 122023: 112024: 132025: 152026 (partial year): 18
2007high 23 (2017) · low 8 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HSB

106in 2025

2007: 68 days median2008: 57 days median2009: 86 days median2010: 117 days median2011: 78 days median2012: 112 days median2013: 105 days median2014: 147 days median2015: 111 days median2016: 124 days median2017: 119 days median2018: 134 days median2019: 132 days median2020: 112 days median2021: 94 days median2022: 172 days median2023: 162 days median2024: 195 days median2025: 106 days median2026 (partial year): 151 days median
2007high 195 (2024) · low 57 (2008)2026

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

Recalls per year · HSB

18in 2025

2008: 92009: 812010: 182011: 22012: 72013: 142014: 32015: 32016: 62017: 662018: 562019: 62020: 62021: 22022: 12023: 12024: 12025: 182026 (partial year): 1
2007high 81 (2009) · low 0 (2007)2026

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

Adverse event reports per year · HSB

2,911in 2025

2007: 1622008: 1842009: 3342010: 4542011: 6622012: 1,0792013: 1,7732014: 1,4742015: 1,6712016: 1,9202017: 1,4472018: 3,5262019: 2,5172020: 3,2992021: 4,1112022: 2,7332023: 2,2192024: 2,8692025: 2,911
2007high 4,111 (2021) · low 162 (2007)2025

MAUDE reports naming product code HSB, 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
20078680162
200811579184
2009188681334
20101411718454
201116782662
20121711271,079
201318105141,773
20141914731,474
20152211131,671
2016812461,920
201723119661,447
201817134563,526
20191313262,517
20201711263,299
2021109424,111
20221217212,733
20231116212,219
20241319512,869
202515106182,911
2026181511—

What is it indicated for?

The AOS ESTm Trochanteric Nail is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric, intertrochanteric and high subtrochanteric, fractures and combinations of these fractures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K103533: ES Trochanteric Nail, Left and Right, 10MM.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K103533

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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