510(k) Report

510(k) · Cleared

Cleared

Texas Scottish Rite Easy/Lock Fixator

K931578510(k) TraditionalCleared Feb 22, 1994329-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

Applied Osteo Systems, Inc. · JEC Component, Traction, Invasive

Cleared on Feb 22, 1994 after a 329-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Feb 22, 1994
Review
329 days
Class
Class II
Product code
JEC
Recalls
None
Predicates
0

FDA has not posted a summary or statement for it, so its predicates are not known.

FIG. 1 — Lineage of K931578Source: FDA 510(k) database · 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in JEC? 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 JEC device

  1. #1 K193256 Anjon Bremer Halo Systemscore 3.2 · 2 generations · no Class I recall
  2. #2 Held for the reportin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

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 JEC devices

JEC Component, Traction, Invasive: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JEC

1in 2021

2007: 12008: 12009: 12011: 12014: 12016: 12018: 22019: 12020: 12021: 1
2007high 2 (2018) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JEC

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

Recalls per year · JEC

1in 2019

2008: 12016: 12018: 12019: 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · JEC

2in 2025

2007: 12008: 92009: 42010: 132011: 152012: 142013: 102014: 62015: 12016: 82017: 122018: 22019: 32020: 62021: 22022: 32023: 262024: 22025: 2
2007high 26 (2023) · low 1 (2007)2025

MAUDE reports naming product code JEC, 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
20071—01
20081—19
20091—04
20100—013
20111—015
20120—014
20130—010
20141—06
20150—01
20161—18
20170—012
20182—12
20191—13
20201—06
20211—02
20220—03
20230—026
20240—02
20250—02
20260—0—
Cite this page

510(k) Report. “K931578: Texas Scottish Rite Easy/Lock Fixator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K931578

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