510(k) Report

PMA · Approved

Approved

Scandinavian Total Ankle Replacement (STAR Ankle)

P050050/S022PMAApproved Mar 11, 202238-day reviewClass III

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

Djo Global · NTG Prosthesis, Ankle, Uncemented, Non-Constrained

Approved on Mar 11, 2022 through premarket approval, which rests on the device’s own clinical evidence after a 38-day review.

Decided
Mar 11, 2022
Review
38 days
Class
Class III
Product code
NTG
Recalls
None

PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.

FIG. 1 — Lineage of P050050/S022Source: FDA PMA database · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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
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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)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

How does its category compare?

All NTG devices

NTG Prosthesis, Ankle, Uncemented, Non-Constrained: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · NTG

2in 2024

2009: 12010: 22013: 22014: 22016: 22018: 12019: 32020: 22021: 72022: 42023: 22024: 22026 (partial year): 1
2007high 7 (2021) · low 0 (2007)2026

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

2018: 22023: 12026 (partial year): 1
2007high 2 (2018) · low 0 (2007)2026

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

Adverse event reports per year · NTG

14in 2025

2009: 22010: 192011: 152012: 192013: 302014: 922015: 3412016: 862017: 822018: 932019: 1292020: 5452021: 892022: 502023: 122024: 222025: 14
2007high 545 (2020) · low 0 (2007)2025

MAUDE reports naming product code NTG, 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
20070—00
20080—00
20091—02
20102—019
20110—015
20120—019
20132—030
20142—092
20150—0341
20162—086
20170—082
20181—293
20193—0129
20202—0545
20217—089
20224—050
20232—112
20242—022
20250—014
20261—1—
Cite this page

510(k) Report. “P050050/S022: Scandinavian Total Ankle Replacement (STAR Ankle).” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P050050/S022

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026