510(k) · Cleared
ClearedHoffmann LRF System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Stryker GmbH · KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Cleared on Dec 21, 2023 as substantially equivalent to K203568 (Stryker GmbH, 2021) after a 29-day review. Its family tree reaches back 10 generations to 2000. 1 later device descends from it.
- Decided
- Dec 21, 2023
- Review
- 29 days
- Class
- Class II
- Product code
- KTT
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 10 generations to K994143 (2000). 14 ancestors in all, the oldest K970748 (1997). 1 later device descends from it, 1 citing it directly.
- Root · 10 generations backK994143 Smith & Nephew External Fixation System [Unilateral (Linear) &…Smith & Nephew, Inc. · 2000 · Recalled
- 6 generations between
- 3 generations backK163656 Hoffmann LRF SystemStryker GmbH · 2017 · Recalled
- 2 generations backK182968 Hoffmann LRF SystemStryker GmbH · 2019
- 1 generation backK203568 Hoffmann LRF SystemStryker GmbH · 2021
- This deviceK233741 Hoffmann LRF SystemStryker GmbH · 2023
- Descendant · cites it directly · 0 of its ownK253202 Hoffmann LRF SystemStryker GmbH · 2025
Show all 10 generations
- Root · 10 generations backK994143 Smith & Nephew External Fixation System [Unilateral (Linear) &…Smith & Nephew, Inc. · 2000 · Recalled
- 9 generations backK031181 External Fixation SystemsSmith & Nephew, Inc. · 2003
- 8 generations backK113327 Hoffmann LRF (Limb Reconstruction Frame) SystemStryker Corp. · 2012 · Recalled
- 7 generations backK130334 Hoffmann LRF (Limb Reconstruction Frame System)Stryker Trauma AG · 2013
- 6 generations backK140961 Hoffmann LRF (Limb Reconstruction Frame) SystemStryker Trauma AG · 2014
- 5 generations backK153377 Hoffmann LRF (Limb Reconstruction Frame) SystemStryker GmbH · 2016 · Recalled
- 4 generations backK161753 Hoffman LRF SystemStryker GmbH · 2016
- 3 generations backK163656 Hoffmann LRF SystemStryker GmbH · 2017 · Recalled
- 2 generations backK182968 Hoffmann LRF SystemStryker GmbH · 2019
- 1 generation backK203568 Hoffmann LRF SystemStryker GmbH · 2021
- This deviceK233741 Hoffmann LRF SystemStryker GmbH · 2023
Most influential descendants
Showing 1 of 1 · See all- K253202Hoffmann LRF SystemStryker GmbH · 2025 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K994143 | Smith & Nephew External Fixation System [Unilateral (Linear) & Multilateral… | Smith & Nephew, Inc. | 2000 | 19 |
| −9 | K031181 | External Fixation Systems | Smith & Nephew, Inc. | 2003 | — |
| −8 | K113327 | Hoffmann LRF (Limb Reconstruction Frame) System | Stryker Corp. | 2012 | 3 |
| −7 | K130334 | Hoffmann LRF (Limb Reconstruction Frame System) | Stryker Trauma AG | 2013 | — |
| −6 | K140961 | Hoffmann LRF (Limb Reconstruction Frame) System | Stryker Trauma AG | 2014 | — |
| −5 | K153377 | Hoffmann LRF (Limb Reconstruction Frame) System | Stryker GmbH | 2016 | 2 |
| −4 | K161753 | Hoffman LRF System | Stryker GmbH | 2016 | — |
| −3 | K163656 | Hoffmann LRF System | Stryker GmbH | 2017 | 5 |
| −2 | K182968 | Hoffmann LRF System | Stryker GmbH | 2019 | — |
| −1 | K203568 | Hoffmann LRF System | Stryker GmbH | 2021 | — |
| 0 (this device) | K233741 | Hoffmann LRF System | Stryker GmbH | 2023 | — |
| +1 | K253202 | Hoffmann LRF System | Stryker GmbH | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
| 2000 | 1 | 0 |
| 2004 | 1 | 0 |
| 2013 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2025 | 1 | 0 |
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 KTT? 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 KTT device
- #1 K242861 TrueLok Elevatescore 21.4 · 14 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K203568 | Hoffmann LRF SystemSummary page 5…accessories (21 CFR § 888.3030) Regulatory Class: Class II Product Code: KTT Primary Predicate: Hoffmann LRF System (K203568) System Description: The Hoffmann LRF System is a modular, ring-based, external fixation system designed to address certain or… | 2021 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K253202 | Hoffmann LRF System | 2025 | 0 |
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 23 years and passes through 4 companies; a new generation was cleared every 1.8 years on median.
- 5 of the 14 ancestors have a recall of any class.
- Of its descendants, K253202 (Stryker GmbH, 2025) has gone furthest, with 0 descendants of its own.
- 1 other device also cites its predicate K203568.
How does its category compare?
All KTT devicesKTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.
FDA decisions per year · KTT
10in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · KTT
88in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KTT
2in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KTT
673in 2025
MAUDE reports naming product code KTT, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 9 | 55 | 2 | 45 |
| 2008 | 11 | 73 | 1 | 66 |
| 2009 | 11 | 94 | 2 | 45 |
| 2010 | 12 | 148 | 1 | 121 |
| 2011 | 10 | 157 | 0 | 196 |
| 2012 | 9 | 140 | 4 | 527 |
| 2013 | 7 | 87 | 7 | 898 |
| 2014 | 14 | 129 | 0 | 445 |
| 2015 | 12 | 60 | 0 | 401 |
| 2016 | 10 | 142 | 0 | 400 |
| 2017 | 11 | 184 | 1 | 485 |
| 2018 | 6 | 149 | 14 | 597 |
| 2019 | 8 | 110 | 3 | 800 |
| 2020 | 9 | 200 | 0 | 942 |
| 2021 | 10 | 83 | 2 | 961 |
| 2022 | 3 | 25 | 0 | 627 |
| 2023 | 7 | 29 | 0 | 554 |
| 2024 | 5 | 90 | 0 | 523 |
| 2025 | 10 | 88 | 0 | 673 |
| 2026 | 5 | 68 | 11 | — |
What is it indicated for?
The Stryker Hoffmann LRF System is indicated in pediatric patients and adults for the treatment and fixation of: Open and closed fractures Post-traumatic joint contracture which has resulted in loss of range of motion Fractures and disease which generally may result in joint contractures or loss of range of motion and fractures requiring distraction Pseudoarthrosis or non-union of long bones Limb lengthening by epiphyseal, diaphyseal, or metaphyseal…
Read the full statement (130 words)
The Stryker Hoffmann LRF System is indicated in pediatric patients and adults for the treatment and fixation of:
Open and closed fractures
Post-traumatic joint contracture which has resulted in loss of range of motion
Fractures and disease which generally may result in joint contractures or loss of range of motion and fractures requiring distraction
Pseudoarthrosis or non-union of long bones
Limb lengthening by epiphyseal, diaphyseal, or metaphyseal distraction
Correction of bony or soft tissue deformity
Correction of segmental bony or soft tissue defects
Joint arthrodesis
Management of comminuted intra-articular fractures of the distal radius
Bone transport
The Hoffmann LRF System is indicated in adults for:
Osteotomy
Revision procedure where other treatments or devices have been unsuccessful
Bone reconstruction procedures
Fusions and replantations of the foot
Charcot foot reconstruction
Lisfranc dislocations
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K233741 · printed Nov 5, 2026
Cite this page
510(k) Report. “K233741: Hoffmann LRF System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K233741
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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