PMA · Approved
Recalled · Class II · 2026Hintermann Series H3 Total Ankle Replacement System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Dt Medtech, LLC · NTG Prosthesis, Ankle, Uncemented, Non-Constrained
Approved on Jun 4, 2019 through premarket approval, which rests on the device’s own clinical evidence after a 1,014-day review. It has been recalled once.
- Decided
- Jun 4, 2019
- Review
- 1,014 days
- Class
- Class III
- Product code
- NTG
- Recalls
- 1
PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.
P160036 has 6 supplements since 2019: changes to the approved device, its labelling or its manufacturing, each approved separately.
PMA supplements approved per year
View FIG. 1 as a table
| Year | Supplements approved |
|---|---|
| 2019 | 1 |
| 2021 | 2 |
| 2023 | 1 |
| 2024 | 1 |
| 2026 | 1 |
Sources: FDA PMA database (decision fields and supplements), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in NTG? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
Does it have a predicate?
PMA decisions do not claim a predicate device.
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Mar 24, 2026 | Class II | Z-2399-2026 | Labeling Change Control | Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device. |
No ancestor or descendant has a Class I recall.
How does its category compare?
All NTG devicesNTG Prosthesis, Ankle, Uncemented, Non-Constrained: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.
FDA decisions per year · NTG
2in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · NTG
Too few NTG 510(k)s in any year since 2007 to give a median.
Recalls per year · NTG
1in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NTG
14in 2025
MAUDE reports naming product code NTG, 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 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 1 | — | 0 | 2 |
| 2010 | 2 | — | 0 | 19 |
| 2011 | 0 | — | 0 | 15 |
| 2012 | 0 | — | 0 | 19 |
| 2013 | 2 | — | 0 | 30 |
| 2014 | 2 | — | 0 | 92 |
| 2015 | 0 | — | 0 | 341 |
| 2016 | 2 | — | 0 | 86 |
| 2017 | 0 | — | 0 | 82 |
| 2018 | 1 | — | 2 | 93 |
| 2019 | 3 | — | 0 | 129 |
| 2020 | 2 | — | 0 | 545 |
| 2021 | 7 | — | 0 | 89 |
| 2022 | 4 | — | 0 | 50 |
| 2023 | 2 | — | 1 | 12 |
| 2024 | 2 | — | 0 | 22 |
| 2025 | 0 | — | 0 | 14 |
| 2026 | 1 | — | 1 | — |
https://510kreport.com/device/P160036 · printed Nov 6, 2026
Cite this page
510(k) Report. “P160036: Hintermann Series H3 Total Ankle Replacement System.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P160036
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026