510(k) Report

510(k) · Cleared

Cleared

Smart Toe II, X Fuse

K201715510(k) TraditionalCleared Aug 5, 202043-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

Stryker GmbH · HTY Pin, Fixation, Smooth

Cleared on Aug 5, 2020 as substantially equivalent to K112197 (Memometal Technologies, 2011) after a 43-day review. Its family tree reaches back 4 generations to 1996. 1 later device descends from it.

Decided
Aug 5, 2020
Review
43 days
Class
Class II
Product code
HTY
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K960385 (1996). 6 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK960385 Sterile Kirschner Wires and Steinmann PinsDepuy, Inc. · 1996
  2. 3 generations backK022599 Newdeal K WireNew Deal, S.A. · 2002
  3. 2 generations backK070598 Memometal Intra-Medullary Bone Fastener, Models Smart Toe / X-FuseMemometal Technologies · 2007
  4. 1 generation backK112197 Memometal Intra-Medullary Bone FastenerMemometal Technologies · 2011 · Recalled
  5. This deviceK201715 Smart Toe II, X FuseStryker GmbH · 2020
  6. Descendant · cites it directly · 0 of its ownK253325 ZipToe™ Hammertoe Fusion SystemToetal Solutions · 2025

Most influential descendants

Showing 1 of 1 · See all
  • K253325ZipToe™ Hammertoe Fusion SystemToetal Solutions · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K960385Sterile Kirschner Wires and Steinmann PinsDepuy, Inc.1996—
−3K022599Newdeal K WireNew Deal, S.A.2002—
−2K070598Memometal Intra-Medullary Bone Fastener, Models Smart Toe / X-FuseMemometal Technologies2007—
−1K112197Memometal Intra-Medullary Bone FastenerMemometal Technologies20111
0 (this device)K201715Smart Toe II, X FuseStryker GmbH2020—
+1K253325ZipToe™ Hammertoe Fusion SystemToetal Solutions2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199710
199810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K201715, 1996–2025Source: 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 HTY? 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 HTY device

  1. #1 K231272 OSSIOfiber® Pin Product Family, OSSIOfiber®…score 19.3 · 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? (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
*K112197Memometal Intra-Medullary Bone Fastener
Summary page 5
…June 22, 2020 Primary Predicate: Memometal Intramedullary Bone Fastener (Smart Toe/X Fuse) (K112197) Reference Devices: Memory Metal Staples, Easyclip (K122113) Description The Smart Toe II & X Fuse, previo…
Memometal Technologies20111
†K122113Memory Metal Staples, EasyclipStryker Corp.20131

Also cleared against K112197: 3 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K253325ZipToe™ Hammertoe Fusion SystemToetal Solutions20250

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 24 years and passes through 4 companies; a new generation was cleared every 6.6 years on median.
  • 1 of the 6 ancestors has a recall of any class.
  • Of its descendants, K253325 (Toetal Solutions, 2025) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K112197.

How does its category compare?

All HTY devices

HTY Pin, Fixation, Smooth: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · HTY

5in 2025

2007: 62008: 62009: 22010: 92011: 62012: 42013: 42014: 82015: 82016: 62017: 52018: 42019: 42020: 52021: 52022: 42023: 52024: 12025: 52026 (partial year): 2
2007high 9 (2010) · low 1 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HTY

90in 2025

2007: 112 days median2008: 86 days median2010: 180 days median2011: 82 days median2012: 76 days median2013: 128 days median2014: 73 days median2015: 101 days median2016: 114 days median2017: 127 days median2018: 162 days median2019: 93 days median2020: 108 days median2021: 137 days median2022: 121 days median2023: 146 days median2025: 90 days median
2007high 180 (2010) · low 73 (2014)2026

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

Recalls per year · HTY

2in 2022

2009: 12010: 12016: 22019: 12022: 22026 (partial year): 1
2007high 2 (2016) · low 0 (2007)2026

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

Adverse event reports per year · HTY

39in 2025

2007: 462008: 382009: 362010: 332011: 1642012: 1292013: 1872014: 1492015: 1212016: 1282017: 822018: 1382019: 2222020: 2102021: 1482022: 962023: 1532024: 2972025: 39
2007high 297 (2024) · low 33 (2010)2025

MAUDE reports naming product code HTY, 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
20076112046
2008686038
20092—136
20109180133
20116820164
20124760129
201341280187
20148730149
201581010121
201661142128
20175127082
201841620138
20194931222
202051080210
202151370148
20224121296
202351460153
20241—0297
2025590039
20262—1—

What is it indicated for?

The Smart Toe II is indicated for interphalangeal fusion of the toes.

The X Fuse is indicated for interphalangeal fusion of fingers and toes.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K201715: Smart Toe II, X Fuse.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K201715

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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