510(k) Report

510(k) · Cleared

Cleared

Conquest FN

K152686510(k) TraditionalCleared Mar 17, 2016181-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

Smith & Nephew · JDO Device, Fixation, Proximal Femoral, Implant

Cleared on Mar 17, 2016 as substantially equivalent to K102057 (Aesculap Implant Systems, LLC, 2010) and 2 other predicates after a 181-day review. Its family tree reaches back 10 generations to 1996. 12 later devices descend from it.

Decided
Mar 17, 2016
Review
181 days
Class
Class II
Product code
JDO
Recalls
None
Predicates
3

Its longest line of descent runs back 10 generations to K962616 (1996). 73 ancestors in all, the oldest K792022 (1979). 12 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2010: 2 other ancestors2008: 2 other ancestors2007: 2 other ancestors2006: 4 other ancestors2005: 5 other ancestors2002: 4 other ancestors2001: 7 other ancestors1996: 6 other ancestors2003: 2 other ancestors2000: 7 other ancestors1999: 5 other ancestors1998: 3 other ancestors1995: 2 other ancestors1990: 1 other ancestor1979: 1 other ancestor2004: 4 other ancestors1994: 2 other ancestors1993: 2 other ancestors1991: 1 other ancestor1989: 1 other ancestor2020: 1 descendant cleared2022: 1 descendant cleared2017: 1 descendant cleared2021: 2 descendants cleared2025: 2 descendants cleared2023: 3 descendants cleared2026: 2 descendants clearedK962616 · Synthes Dorsal Distal Radius Plate (DDRP) System · Synthes (Usa) · 1996K982732 · Synthes (Usa) Distal Radius Plate System (DRPS) · Synthes · 1998×3: 3 generations cleared close together, K023007 (2002), K030198 (2003), K032705 (2003) ×2: 2 generations cleared close together, K050932 (2005), K051735 (2005) K071563 · Peri-Loc Periarticular Locked Plating System · Smith & Nephew, Inc. · 2007K090675 · Smith & Nephew, Inc. VLP Foot Plating, Screw System and Accessories · Smith & Nephew, Inc. · 2009K111994 · Smith & Nephew Cannulated Screws and Washers · Smith & Nephew, Inc. · 201119801990200020102020
  1. Root · 10 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
  2. 6 generations between
  3. 3 generations backK071563 Peri-Loc Periarticular Locked Plating SystemSmith & Nephew, Inc. · 2007
  4. 2 generations backK090675 Smith & Nephew, Inc. VLP Foot Plating, Screw System and AccessoriesSmith & Nephew, Inc. · 2009
  5. 1 generation backK111994 Smith & Nephew Cannulated Screws and WashersSmith & Nephew, Inc. · 2011
  6. This deviceK152686 Conquest FNSmith & Nephew · 2016
  7. Descendant · cites it directly · 10 of its ownK193029 Conquest FNSmith & Nephew, Inc. · 2020
  8. Descendant · cites it directly · 8 of its ownK172785 Conquest FNSmith & Nephew · 2017
  9. Descendant · cites it directly · 7 of its ownK210837 Smith & Nephew Plates and ScrewsSmith & Nephew, Inc. · 2021 · Recalled
  10. Descendant · cites it directly · 2 of its ownK213126 Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc…Smith & Nephew, Inc. · 2022 · Recalled
  11. Descendant · 2 generations on · 1 of its ownK233017 TM Plating SystemTyber Medical, LLC · 2023
Show all 10 generations
  1. Root · 10 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
  2. 9 generations backK982732 Synthes (Usa) Distal Radius Plate System (DRPS)Synthes · 1998
  3. 8 generations backK023007 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2002
  4. 7 generations backK030198 Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
  5. 6 generations backK032705 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
  6. 5 generations backK050932 Distal Volar Radius Anatomical Plate SystemHand Innovations, Inc. · 2005 · Recalled
  7. 4 generations backK051735 Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper…Smith & Nephew, Inc. · 2005
  8. 3 generations backK071563 Peri-Loc Periarticular Locked Plating SystemSmith & Nephew, Inc. · 2007
  9. 2 generations backK090675 Smith & Nephew, Inc. VLP Foot Plating, Screw System and AccessoriesSmith & Nephew, Inc. · 2009
  10. 1 generation backK111994 Smith & Nephew Cannulated Screws and WashersSmith & Nephew, Inc. · 2011
  11. This deviceK152686 Conquest FNSmith & Nephew · 2016

Showing 5 of 12 descendants. See all descendants

Descendants cleared per year

2017: 12020: 12021: 22022: 12023: 32025: 22026: 2
2017high 3 (2023) · low 0 (2018)2026

Most influential descendants

Showing 5 of 12 · See all
  • K193029Conquest FNSmith & Nephew, Inc. · 2020 · cites it directly10descendants
  • K172785Conquest FNSmith & Nephew · 2017 · cites it directly8descendants
  • K210837Smith & Nephew Plates and ScrewsSmith & Nephew, Inc. · 2021 · cites it directly7descendants
  • K213126Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP…Smith & Nephew, Inc. · 2022 · cites it directly2descendants
  • K233017TM Plating SystemTyber Medical, LLC · 2023 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K962616Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa)1996—
−9K982732Synthes (Usa) Distal Radius Plate System (DRPS)Synthes1998—
−8K023007Distal Radius Fracture Repair SystemHand Innovations, Inc.2002—
−7K030198Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc.2003—
−6K032705Distal Radius Fracture Repair SystemHand Innovations, Inc.2003—
−5K050932Distal Volar Radius Anatomical Plate SystemHand Innovations, Inc.20051
−4K051735Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper ExtremitySmith & Nephew, Inc.2005—
−3K071563Peri-Loc Periarticular Locked Plating SystemSmith & Nephew, Inc.2007—
−2K090675Smith & Nephew, Inc. VLP Foot Plating, Screw System and AccessoriesSmith & Nephew, Inc.2009—
−1K111994Smith & Nephew Cannulated Screws and WashersSmith & Nephew, Inc.2011—
0 (this device)K152686Conquest FNSmith & Nephew2016—
+1K193029Conquest FNSmith & Nephew, Inc.2020—
+1K172785Conquest FNSmith & Nephew2017—
+1K210837Smith & Nephew Plates and ScrewsSmith & Nephew, Inc.20211
+1K213126Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100…Smith & Nephew, Inc.20221
+2K233017TM Plating SystemTyber Medical, LLC2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198910
199010
199110
199320
199420
199520
199660
199830
199950
200070
200170
200240
200320
200440
200550
200640
200720
200820
201020

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
202010
202120
202210
202330
202520
202620
FIG. 1 — Lineage of K152686, 1996–2026Source: 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 JDO? 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 JDO device

  1. #1 K213126 Smith & Nephew, Inc. Plates and Screws…score 12.0 · 14 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? (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
*K102057Targon FN System
Summary page 4
…regard to intended use, indications for use, and performance characteristics. The subject CONQUEST FN features characteristics very similar to the Targon FN cleared via K102057, with the primary differences being material changes and the utilization of POGO Screw technology (K080649). To accommodate for d…
Aesculap Implant Systems, LLC2010—
*K080649Pogo Screw
Summary page 4
…ures characteristics very similar to the Targon FN cleared via K102057, with the primary differences being material changes and the utilization of POGO Screw technology (K080649). To accommodate for differences between the subject device and the predicate cleared via K102057, mechanical testing was conduct…
Fxdevices2008—
*K111994Smith & Nephew Cannulated Screws and Washers
Summary page 5
…K080649 11/25/08 Smith & Nephew Cannulated Screws and Smith & Nephew K111994 10/11/2011 Washers Summary of Pre-Clinical Testing • Axial Pullout Strength Evaluation was c…
Smith & Nephew, Inc.2011—

Also cleared against K102057: 1 other device →

What descends from it? (12)

See all 12

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

NumberDeviceApplicantDecidedDescendants
K193029Conquest FNSmith & Nephew, Inc.202010
K172785Conquest FNSmith & Nephew20178
K210837Smith & Nephew Plates and ScrewsSmith & Nephew, Inc.20217
K213126Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP…Smith & Nephew, Inc.20222

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 20 years and passes through 5 companies; a new generation was cleared every 2.1 years on median.
  • 15 of the 73 ancestors have a recall of any class.
  • Of its descendants, K193029 (Smith & Nephew, Inc., 2020) has gone furthest, with 10 descendants of its own.
  • 1 other device also cites its predicate K102057.

How does its category compare?

All JDO devices

JDO Device, Fixation, Proximal Femoral, Implant: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.

FDA decisions per year · JDO

1in 2023

2008: 22014: 12016: 12017: 12018: 12020: 12021: 12022: 12023: 12026 (partial year): 1
2007high 2 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JDO

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

Recalls per year · JDO

1in 2013

2013: 1
2007high 1 (2013) · low 0 (2007)2026

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

Adverse event reports per year · JDO

1in 2025

2007: 42008: 12009: 12010: 62011: 62012: 92013: 522014: 152015: 192016: 442017: 262018: 182019: 102020: 192021: 102022: 32023: 52024: 22025: 1
2007high 52 (2013) · low 1 (2008)2025

MAUDE reports naming product code JDO, 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
20070—04
20082—01
20090—01
20100—06
20110—06
20120—09
20130—152
20141—015
20150—019
20161—044
20171—026
20181—018
20190—010
20201—019
20211—010
20221—03
20231—05
20240—02
20250—01
20261—0—

What is it indicated for?

The Smith & Nephew CONQUEST FN is indicated for displaced and undisplaced intracapsular femoral neck fractures.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K152686: Conquest FN.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K152686

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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