510(k) Report

510(k) · Cleared

Cleared

Align Anterior Ankle Fusion Plate

K160191510(k) TraditionalCleared Mar 25, 201658-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

Extremity Medical, LLC · HRS Plate, Fixation, Bone

Cleared on Mar 25, 2016 as substantially equivalent to K081934 (Extremity Medical, LLC, 2008) and 3 other predicates after a 58-day review. Its family tree reaches back 13 generations to 1996. 5 later devices descend from it.

Decided
Mar 25, 2016
Review
58 days
Class
Class II
Product code
HRS
Recalls
None
Predicates
4

Its longest line of descent runs back 13 generations to K954385 (1996). 157 ancestors in all, the oldest K792022 (1979). 5 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2014: 1 other ancestor2012: 2 other ancestors2008: 7 other ancestors2011: 2 other ancestors2010: 7 other ancestors2009: 8 other ancestors2006: 13 other ancestors2005: 11 other ancestors2003: 6 other ancestors2001: 14 other ancestors2000: 12 other ancestors1995: 4 other ancestors2007: 5 other ancestors2004: 5 other ancestors2002: 14 other ancestors1999: 5 other ancestors1996: 8 other ancestors1998: 6 other ancestors1994: 5 other ancestors1979: 1 other ancestor1992: 2 other ancestors1991: 1 other ancestor1990: 1 other ancestor1989: 1 other ancestor1993: 2 other ancestors1997: 1 other ancestor2018: 1 descendant cleared2023: 1 descendant cleared2021: 1 descendant cleared2022: 1 descendant cleared2026: 1 descendant clearedK954385 · Synthes Mandibular Modular Fixation System · Synthes (Usa) · 1996K974555 · Synthes 2.0 MM Locking Plate System (2.0 LPS) · Synthes (Usa) · 1998×2: 2 generations cleared close together, K030448 (2003), K032442 (2003) K040598 · KLS Martin Hand Plating System · KLS-Martin L.P. · 2004K050868 · Maxlock · Orthohelix Surgical Designs, Inc. · 2005K073624 · Modular Foot System · Orthohelix Surgical Designs, Inc. · 2008 · recalled×2: 2 generations cleared close together, K100618 (2010), K102156 (2010) K113048 · Maxlock Extreme System · Orthohelix Surgical Designs, Inc. · 2012×2: 2 generations cleared close together, K122005 (2012), K123203 (2012) K132591 · Maxlock Extreme System · Orthohelix Surgical Designs, Inc. · 201319801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 3 other ancestors2 generations back: 14 other ancestors3 generations back: 22 other ancestors4 generations back: 22 other ancestors5 generations back: 26 other ancestors6 generations back: 18 other ancestors7 generations back: 11 other ancestors8 generations back: 8 other ancestors9 generations back: 8 other ancestors10 generations back: 6 other ancestors11 generations back: 5 other ancestors12 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 2 descendants3 generations forward: 2 descendants K132591 · Maxlock Extreme System · Orthohelix Surgical Designs, Inc. · 2013K123203 · Maxlock Extreme System Model MXL · Orthohelix Surgical Designs, Inc. · 2012K122005 · Maxlock Extreme System · Orthohelix Surgical Designs, Inc. · 2012K113048 · Maxlock Extreme System · Orthohelix Surgical Designs, Inc. · 2012K102156 · Maxlock Extreme Extremity Plating System Distal Radius Plates and Screws · Orthohelix Surgical Designs, Inc. · 2010 · recalledK100618 · Maxlock Extreme Extremity Plating System with Variable Angle Technology · Orthohelix Surgical Designs, Inc. · 2010K073624 · Modular Foot System · Orthohelix Surgical Designs, Inc. · 2008 · recalledK050868 · Maxlock · Orthohelix Surgical Designs, Inc. · 2005K040598 · KLS Martin Hand Plating System · KLS-Martin L.P. · 2004K032442 · KLS-Martin Mandibular/Reconstruction System II · KLS-Martin L.P. · 2003K030448 · Osteomed 2.0 Locking Plates and Screws · Osteomed LP · 2003K974555 · Synthes 2.0 MM Locking Plate System (2.0 LPS) · Synthes (Usa) · 1998K954385 · Synthes Mandibular Modular Fixation System · Synthes (Usa) · 1996−10−50
  1. Root · 13 generations backK954385 Synthes Mandibular Modular Fixation SystemSynthes (Usa) · 1996
  2. 9 generations between
  3. 3 generations backK122005 Maxlock Extreme SystemOrthohelix Surgical Designs, Inc. · 2012
  4. 2 generations backK123203 Maxlock Extreme System Model MXLOrthohelix Surgical Designs, Inc. · 2012
  5. 1 generation backK132591 Maxlock Extreme SystemOrthohelix Surgical Designs, Inc. · 2013
  6. This deviceK160191 Align Anterior Ankle Fusion PlateExtremity Medical, LLC · 2016
  7. Descendant · cites it directly · 4 of its ownK181067 AlignX Ankle Fusion SystemExtremity Medical, LLC · 2018
  8. Descendant · 2 generations on · 1 of its ownK231887 ARIX Ankle Distal Tibia SystemJeil Medical Corporation · 2023
  9. Descendant · 2 generations on · 1 of its ownK212297 Omni Foot and Ankle Plating SystemExtremity Medical, LLC · 2021
  10. Descendant · 3 generations on · 0 of its ownK252246 Leforte MMF SystemJeil Medical Corporation · 2026
  11. Descendant · 3 generations on · 0 of its ownK221362 Omni Foot and Ankle Plating SystemExremity Medical, LLC · 2022
Show all 13 generations
  1. Root · 13 generations backK954385 Synthes Mandibular Modular Fixation SystemSynthes (Usa) · 1996
  2. 12 generations backK974555 Synthes 2.0 MM Locking Plate System (2.0 LPS)Synthes (Usa) · 1998
  3. 11 generations backK030448 Osteomed 2.0 Locking Plates and ScrewsOsteomed LP · 2003
  4. 10 generations backK032442 KLS-Martin Mandibular/Reconstruction System IIKLS-Martin L.P. · 2003
  5. 9 generations backK040598 KLS Martin Hand Plating SystemKLS-Martin L.P. · 2004
  6. 8 generations backK050868 MaxlockOrthohelix Surgical Designs, Inc. · 2005
  7. 7 generations backK073624 Modular Foot SystemOrthohelix Surgical Designs, Inc. · 2008 · Recalled
  8. 6 generations backK100618 Maxlock Extreme Extremity Plating System with Variable Angle…Orthohelix Surgical Designs, Inc. · 2010
  9. 5 generations backK102156 Maxlock Extreme Extremity Plating System Distal Radius Plates and…Orthohelix Surgical Designs, Inc. · 2010 · Recalled
  10. 4 generations backK113048 Maxlock Extreme SystemOrthohelix Surgical Designs, Inc. · 2012
  11. 3 generations backK122005 Maxlock Extreme SystemOrthohelix Surgical Designs, Inc. · 2012
  12. 2 generations backK123203 Maxlock Extreme System Model MXLOrthohelix Surgical Designs, Inc. · 2012
  13. 1 generation backK132591 Maxlock Extreme SystemOrthohelix Surgical Designs, Inc. · 2013
  14. This deviceK160191 Align Anterior Ankle Fusion PlateExtremity Medical, LLC · 2016

Most influential descendants

Showing 5 of 5 · See all
  • K181067AlignX Ankle Fusion SystemExtremity Medical, LLC · 2018 · cites it directly4descendants
  • K231887ARIX Ankle Distal Tibia SystemJeil Medical Corporation · 2023 · 2 generations on1descendant
  • K212297Omni Foot and Ankle Plating SystemExtremity Medical, LLC · 2021 · 2 generations on1descendant
  • K252246Leforte MMF SystemJeil Medical Corporation · 2026 · 3 generations on0descendants
  • K221362Omni Foot and Ankle Plating SystemExremity Medical, LLC · 2022 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K954385Synthes Mandibular Modular Fixation SystemSynthes (Usa)1996—
−12K974555Synthes 2.0 MM Locking Plate System (2.0 LPS)Synthes (Usa)1998—
−11K030448Osteomed 2.0 Locking Plates and ScrewsOsteomed LP2003—
−10K032442KLS-Martin Mandibular/Reconstruction System IIKLS-Martin L.P.2003—
−9K040598KLS Martin Hand Plating SystemKLS-Martin L.P.2004—
−8K050868MaxlockOrthohelix Surgical Designs, Inc.2005—
−7K073624Modular Foot SystemOrthohelix Surgical Designs, Inc.20081
−6K100618Maxlock Extreme Extremity Plating System with Variable Angle TechnologyOrthohelix Surgical Designs, Inc.2010—
−5K102156Maxlock Extreme Extremity Plating System Distal Radius Plates and ScrewsOrthohelix Surgical Designs, Inc.20101
−4K113048Maxlock Extreme SystemOrthohelix Surgical Designs, Inc.2012—
−3K122005Maxlock Extreme SystemOrthohelix Surgical Designs, Inc.2012—
−2K123203Maxlock Extreme System Model MXLOrthohelix Surgical Designs, Inc.2012—
−1K132591Maxlock Extreme SystemOrthohelix Surgical Designs, Inc.2013—
0 (this device)K160191Align Anterior Ankle Fusion PlateExtremity Medical, LLC2016—
+1K181067AlignX Ankle Fusion SystemExtremity Medical, LLC2018—
+2K231887ARIX Ankle Distal Tibia SystemJeil Medical Corporation2023—
+2K212297Omni Foot and Ankle Plating SystemExtremity Medical, LLC2021—
+3K252246Leforte MMF SystemJeil Medical Corporation2026—
+3K221362Omni Foot and Ankle Plating SystemExremity Medical, LLC2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198910
199010
199110
199220
199320
199450
199540
199680
199710
199860
199950
2000120
2001140
2002140
200360
200450
2005110
2006130
200750
200870
200980
201070
201120
201220
201410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201810
202110
202210
202310
202610
FIG. 1 — Lineage of K160191, 1996–2026Source: 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), 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 HRS? 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 HRS device

  1. #1 K222465 Tyber Medical Anatomical Plating Systemscore 27.5 · 16 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? (4)

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
*K081934Extremity Medical Compression Screw
Summary page 4
…3040 - Smooth or threaded metallic bone fixation fastener Number Product Code HRS (plate, fixation, bone); HWC (screw, fixation, bone) K081934 – Extremity Medical Compression Screw Predicate K133691 – Extremilock Ankle Plating System Devices…
Extremity Medical, LLC2008—
*K133691Extrimilock Ankle Plating System
Summary page 4
…ct Code HRS (plate, fixation, bone); HWC (screw, fixation, bone) K081934 – Extremity Medical Compression Screw Predicate K133691 – Extremilock Ankle Plating System Devices K132591 – Maxlock Extreme System K121425 – Ort…
Osteomed LP2014—
*K132591Maxlock Extreme System
Summary page 4
…n, bone) K081934 – Extremity Medical Compression Screw Predicate K133691 – Extremilock Ankle Plating System Devices K132591 – Maxlock Extreme System K121425 – Ortholoc 3Di Ankle Fusion Plating System and Ortholoc Bone Screws…
Orthohelix Surgical Designs, Inc.2013—
*K121425Ortholoc 3DI Ankle Fusion Plating System
Summary page 4
…cal Compression Screw Predicate K133691 – Extremilock Ankle Plating System Devices K132591 – Maxlock Extreme System K121425 – Ortholoc 3Di Ankle Fusion Plating System and Ortholoc Bone Screws The Align Anterior Ankle Fusion Plat…
Wrightmedicaltechnologyinc2012—

Also cleared against K081934: 3 other devices →

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K181067AlignX Ankle Fusion SystemExtremity Medical, LLC20184

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 1.0 years on median.
  • 28 of the 157 ancestors have a recall of any class.
  • Of its descendants, K181067 (Extremity Medical, LLC, 2018) has gone furthest, with 4 descendants of its own.
  • 3 other devices also cite its predicate K081934.

How does its category compare?

All HRS devices

HRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.

FDA decisions per year · HRS

54in 2025

2007: 352008: 352009: 472010: 492011: 432012: 592013: 562014: 762015: 562016: 442017: 572018: 402019: 462020: 482021: 402022: 472023: 402024: 542025: 542026 (partial year): 51
2007high 76 (2014) · low 35 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HRS

90in 2025

2007: 63 days median2008: 87 days median2009: 85 days median2010: 100 days median2011: 88 days median2012: 106 days median2013: 89 days median2014: 57 days median2015: 97 days median2016: 109 days median2017: 122 days median2018: 116 days median2019: 89 days median2020: 88 days median2021: 87 days median2022: 144 days median2023: 120 days median2024: 96 days median2025: 90 days median2026 (partial year): 82 days median
2007high 144 (2022) · low 57 (2014)2026

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

Recalls per year · HRS

1in 2025

2007: 22008: 112009: 32010: 162011: 52012: 42013: 112015: 72016: 52017: 32018: 22019: 252020: 12021: 92022: 32023: 12025: 12026 (partial year): 3
2007high 25 (2019) · low 0 (2014)2026

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

Adverse event reports per year · HRS

2,306in 2025

2007: 3392008: 3112009: 4352010: 4912011: 7732012: 1,6632013: 2,6432014: 2,4132015: 3,0952016: 2,2762017: 2,2202018: 2,6632019: 3,3592020: 2,7902021: 2,4422022: 1,7002023: 2,0492024: 1,8492025: 2,306
2007high 3,359 (2019) · low 311 (2008)2025

MAUDE reports naming product code HRS, 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
200735632339
2008358711311
200947853435
20104910016491
201143885773
20125910641,663
20135689112,643
2014765702,413
2015569773,095
20164410952,276
20175712232,220
20184011622,663
20194689253,359
2020488812,790
2021408792,442
20224714431,700
20234012012,049
2024549601,849
2025549012,306
202651823—

What is it indicated for?

The Align Anterior Ankle Fusion Plate is intended to facilitate arthrodesis of the ankle including tibiotalocalcaneal and tibiotalar joints.

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. “K160191: Align Anterior Ankle Fusion Plate.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K160191

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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