510(k) Report

510(k) · Cleared

Cleared

CrossTIE Intraosseous Fixation System

K151270510(k) TraditionalCleared Sep 4, 2015114-day reviewClass II21 CFR 888.3040

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

Crossroads Extremity Systems, LLC · HWC Screw, Fixation, Bone

Cleared on Sep 4, 2015 as substantially equivalent to K141857 (Orthodiscovery Group, LLC (D.B.A. Crossroads Extrem, 2015) after a 114-day review. Its family tree reaches back 6 generations to 1990. 15 later devices descend from it.

Decided
Sep 4, 2015
Review
114 days
Class
Class II
Product code
HWC
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K901456 (1990). 33 ancestors in all, the oldest K792670 (1980). 15 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2012: 4 other ancestors2008: 1 other ancestor2007: 4 other ancestors2002: 2 other ancestors1999: 1 other ancestor2010: 1 other ancestor2003: 1 other ancestor2001: 3 other ancestors2000: 2 other ancestors1998: 1 other ancestor1997: 2 other ancestors1996: 2 other ancestors2006: 1 other ancestor2004: 1 other ancestor1980: 1 other ancestor2019: 2 descendants cleared2024: 3 descendants cleared2021: 2 descendants cleared2023: 2 descendants cleared2025: 2 descendants cleared2026: 4 descendants clearedK901456 · Orthosorb (R) Absorbable Pin · Johnson & Johnson International · 1990K031712 · Inion Otps Biodegradable Pin · Inion, Ltd. · 2003K050275 · Modification to: Inion Otps Biodegradable Pin · Inion, Ltd. · 2005K061164 · Activapin · Bioretec, Ltd. · 2006K133636 · Extremity Medical Hammertoe Device · Extremity Medical, LLC · 2014K141857 · CrossTie Intraosseous Fixation System · Orthodiscovery Group, LLC (D.B.A. Crossroads Extrem · 201519801990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 3 other ancestors3 generations back: 7 other ancestors4 generations back: 10 other ancestors5 generations back: 5 other ancestors6 generations back: 2 other ancestors 1 generation forward: 1 descendant2 generations forward: 6 descendants3 generations forward: 4 descendants4 generations forward: 4 descendants K141857 · CrossTie Intraosseous Fixation System · Orthodiscovery Group, LLC (D.B.A. Crossroads Extrem · 2015K133636 · Extremity Medical Hammertoe Device · Extremity Medical, LLC · 2014K061164 · Activapin · Bioretec, Ltd. · 2006K050275 · Modification to: Inion Otps Biodegradable Pin · Inion, Ltd. · 2005K031712 · Inion Otps Biodegradable Pin · Inion, Ltd. · 2003K901456 · Orthosorb (R) Absorbable Pin · Johnson & Johnson International · 1990−50
  1. Root · 6 generations backK901456 Orthosorb (R) Absorbable PinJohnson & Johnson International · 1990
  2. 5 generations backK031712 Inion Otps Biodegradable PinInion, Ltd. · 2003
  3. 4 generations backK050275 Modification to: Inion Otps Biodegradable PinInion, Ltd. · 2005
  4. 3 generations backK061164 ActivapinBioretec, Ltd. · 2006
  5. 2 generations backK133636 Extremity Medical Hammertoe DeviceExtremity Medical, LLC · 2014
  6. 1 generation backK141857 CrossTie Intraosseous Fixation SystemOrthodiscovery Group, LLC (D.B.A. Crossroads Extrem · 2015
  7. This deviceK151270 CrossTIE Intraosseous Fixation SystemCrossroads Extremity Systems, LLC · 2015
  8. Descendant · cites it directly · 14 of its ownK181872 MIS Bunion SystemCrossroads Extremity Systems, LLC · 2019
  9. Descendant · 2 generations on · 7 of its ownK221181 Treace Medical Concepts (TMC) Plating SystemTreace Medical Concepts, Inc. · 2023
  10. Descendant · 2 generations on · 4 of its ownK240173 Treace Medical Systems (TMC) Plating SystemTreace Medical Concepts, Inc. · 2024 · Recalled
  11. Descendant · 2 generations on · 4 of its ownK212487 CoLink Vallux Plating SystemIn2bones USA, LLC · 2021
  12. Descendant · 3 generations on · 3 of its ownK242415 TMC Compression Implant SystemTreace Medical Concepts · 2024

Showing 5 of 15 descendants. See all descendants

Descendants cleared per year

2019: 22021: 22023: 22024: 32025: 22026: 4
2019high 4 (2026) · low 0 (2020)2026

Most influential descendants

Showing 5 of 15 · See all
  • K181872MIS Bunion SystemCrossroads Extremity Systems, LLC · 2019 · cites it directly14descendants
  • K221181Treace Medical Concepts (TMC) Plating SystemTreace Medical Concepts, Inc. · 2023 · 2 generations on7descendants
  • K240173Treace Medical Systems (TMC) Plating SystemTreace Medical Concepts, Inc. · 2024 · 2 generations on4descendants
  • K212487CoLink Vallux Plating SystemIn2bones USA, LLC · 2021 · 2 generations on4descendants
  • K242415TMC Compression Implant SystemTreace Medical Concepts · 2024 · 3 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K901456Orthosorb (R) Absorbable PinJohnson & Johnson International1990—
−5K031712Inion Otps Biodegradable PinInion, Ltd.2003—
−4K050275Modification to: Inion Otps Biodegradable PinInion, Ltd.2005—
−3K061164ActivapinBioretec, Ltd.2006—
−2K133636Extremity Medical Hammertoe DeviceExtremity Medical, LLC2014—
−1K141857CrossTie Intraosseous Fixation SystemOrthodiscovery Group, LLC (D.B.A. Crossroads Extrem2015—
0 (this device)K151270CrossTIE Intraosseous Fixation SystemCrossroads Extremity Systems, LLC2015—
+1K181872MIS Bunion SystemCrossroads Extremity Systems, LLC2019—
+2K221181Treace Medical Concepts (TMC) Plating SystemTreace Medical Concepts, Inc.2023—
+2K240173Treace Medical Systems (TMC) Plating SystemTreace Medical Concepts, Inc.20241
+2K212487CoLink Vallux Plating SystemIn2bones USA, LLC2021—
+3K242415TMC Compression Implant SystemTreace Medical Concepts2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
199620
199720
199810
199910
200020
200130
200220
200310
200410
200610
200740
200810
201010
201240

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201920
202120
202320
202430
202520
202640
FIG. 1 — Lineage of K151270, 1990–2026Source: 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 HWC? 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 HWC device

  1. #1 K203011 Monster Screw Systemscore 22.2 · 14 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? (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
*K141857CrossTie Intraosseous Fixation System
Summary page 4
…21 CFR 888.3040 Classification Class II Appropriate Classification Panel 87 - Orthopedic Predicate Devices K141857 CrossTIE™ Intraosseous Fixation System Reason For Submission Update to Surgical Technique Substantial Equiva…
Orthodiscovery Group, LLC (D.B.A. Crossroads Extrem2015—

What descends from it? (15)

See all 15

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

NumberDeviceApplicantDecidedDescendants
K181872MIS Bunion SystemCrossroads Extremity Systems, LLC201914

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 25 years and passes through 6 companies; a new generation was cleared every 1.5 years on median.
  • 5 of the 33 ancestors have a recall of any class.
  • Of its descendants, K181872 (Crossroads Extremity Systems, LLC, 2019) has gone furthest, with 14 descendants of its own.

How does its category compare?

All HWC devices

HWC Screw, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · HWC

15in 2025

2007: 352008: 332009: 272010: 232011: 352012: 202013: 252014: 312015: 412016: 262017: 402018: 202019: 302020: 282021: 262022: 262023: 242024: 172025: 152026 (partial year): 21
2007high 41 (2015) · low 15 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HWC

111in 2025

2007: 77 days median2008: 76 days median2009: 113 days median2010: 110 days median2011: 88 days median2012: 99 days median2013: 90 days median2014: 88 days median2015: 85 days median2016: 131 days median2017: 127 days median2018: 106 days median2019: 108 days median2020: 75 days median2021: 84 days median2022: 167 days median2023: 104 days median2024: 90 days median2025: 111 days median2026 (partial year): 125 days median
2007high 167 (2022) · low 75 (2020)2026

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

Recalls per year · HWC

1in 2025

2007: 252008: 332009: 292010: 72011: 122012: 302013: 142014: 22015: 52016: 42017: 42018: 12019: 52020: 42021: 22022: 132025: 12026 (partial year): 2
2007high 33 (2008) · low 0 (2023)2026

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

Adverse event reports per year · HWC

2,893in 2025

2007: 6692008: 6602009: 6512010: 7652011: 1,1042012: 3,3392013: 3,8502014: 2,5492015: 2,7112016: 2,2852017: 2,5612018: 3,6622019: 5,4632020: 4,8202021: 4,4462022: 3,9342023: 3,7182024: 3,5752025: 2,893
2007high 5,463 (2019) · low 651 (2009)2025

MAUDE reports naming product code HWC, 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
2007357725669
2008337633660
20092711329651
2010231107765
20113588121,104
20122099303,339
20132590143,850
2014318822,549
2015418552,711
20162613142,285
20174012742,561
20182010613,662
20193010855,463
2020287544,820
2021268424,446
202226167133,934
20232410403,718
2024179003,575
20251511112,893
2026211252—

What is it indicated for?

The CrossTie™ Intraosseous Fixation System is indicated to aid in the fixation of fractures, fusions, and osteotomies of the toes, such as hammertoe, claw toe, mallet toe and inter-digital fusions.

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. “K151270: CrossTIE Intraosseous Fixation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151270

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