510(k) Report

PMA · Approved

Recalled · Class II · 2025

Axsym Free Psa

P980007PMAApproved Feb 5, 20042,159-day reviewClass IIIRecalls 1

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

Abbott Laboratories · MTG Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions

Approved on Feb 5, 2004 through premarket approval, which rests on the device’s own clinical evidence after a 2,159-day review. It has been recalled once.

Decided
Feb 5, 2004
Review
2,159 days
Class
Class III
Product code
MTG
Recalls
1

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

P980007 has 55 supplements since 2004: changes to the approved device, its labelling or its manufacturing, each approved separately.

PMA supplements approved per year

2004: 62007: 12009: 12010: 22011: 132012: 52013: 32014: 62015: 22020: 32021: 32022: 12023: 72025: 12026: 1
2004high 13 (2011) · low 0 (2005)2026
View FIG. 1 as a table
YearSupplements approved
20046
20071
20091
20102
201113
20125
20133
20146
20152
20203
20213
20221
20237
20251
20261
FIG. 1 — Supplements to P980007, 2004–2026Source: FDA PMA database

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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 MTG? 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)

Recalls of this device

DateClassRecallRoot causeReason
Apr 24, 2025Class IIZ-1852-2025Storagetransit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test…

No ancestor or descendant has a Class I recall.

How does its category compare?

All MTG devices

MTG Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MTG

6in 2025

2007: 72008: 72009: 32010: 92011: 252012: 172013: 122014: 132015: 72016: 32017: 92018: 72019: 92020: 132021: 72022: 42023: 92024: 32025: 62026 (partial year): 6
2007high 25 (2011) · low 3 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MTG

Too few MTG 510(k)s in any year since 2007 to give a median.

Recalls per year · MTG

1in 2011

2008: 12011: 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · MTG

20in 2025

2011: 32012: 42013: 32014: 12015: 92016: 52017: 82018: 122019: 132020: 62021: 92022: 42023: 52024: 82025: 20
2007high 20 (2025) · low 0 (2007)2025

MAUDE reports naming product code MTG, 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
20077—00
20087—10
20093—00
20109—00
201125—13
201217—04
201312—03
201413—01
20157—09
20163—05
20179—08
20187—012
20199—013
202013—06
20217—09
20224—04
20239—05
20243—08
20256—020
20266—0—
Cite this page

510(k) Report. “P980007: Axsym Free Psa.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P980007

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