510(k) Report

510(k) · Cleared

Cleared

Cryomedics Neurostat

K831963510(k) TraditionalCleared Aug 12, 198356-day reviewClass II21 CFR 882.4250

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

Spembly Medical, Ltd. · GXH Device, Surgical, Cryogenic

Cleared on Aug 12, 1983 after a 56-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 23 later devices descend from it.

Decided
Aug 12, 1983
Review
56 days
Class
Class II
Product code
GXH
Recalls
None
Predicates
0

23 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2003: 1 descendant cleared2010: 2 descendants cleared2014: 2 descendants cleared2005: 1 descendant cleared2012: 1 descendant cleared2013: 1 descendant cleared2016: 1 descendant cleared2018: 4 descendants cleared2024: 2 descendants cleared2026: 1 descendant cleared2020: 1 descendant cleared2015: 1 descendant cleared2025: 1 descendant cleared2023: 1 descendant cleared2017: 1 descendant cleared2021: 1 descendant cleared2022: 1 descendant cleared19801990200020102020
  1. This deviceK831963 Cryomedics NeurostatSpembly Medical, Ltd. · 1983
  2. Descendant · cites it directly · 22 of its ownK031482 Cryostar System, Comprising: a) Cryostar Console, B) Cryostar 1MM…Cryomedical Instruemts, Ltd. · 2003
  3. Descendant · 2 generations on · 11 of its ownK050272 Cryomedical Instruments Cryo-Pac SystemsCryomedical Instruments, Ltd. · 2005
  4. Descendant · cites it directly · 10 of its ownK100447 Myoscience Cryo-TouchMyoscience, Inc. · 2010
  5. Descendant · 2 generations on · 9 of its ownK142203 Atricure Cryo Module System; cryoICE cryoablation probeAtriCure, Inc. · 2014
  6. Descendant · 2 generations on · 9 of its ownK102021 Cryo-Touch IIMyoscience, Inc. · 2010

Showing 5 of 23 descendants. See all descendants

Descendants cleared per year

2003: 12005: 12010: 22012: 12013: 12014: 22015: 12016: 12017: 12018: 42020: 12021: 12022: 12023: 12024: 22025: 12026: 1
2003high 4 (2018) · low 0 (2004)2026

Most influential descendants

Showing 5 of 23 · See all
  • K031482Cryostar System, Comprising: a) Cryostar Console, B) Cryostar 1MM Cryoprobe, C) Cryostar…Cryomedical Instruemts, Ltd. · 2003 · cites it directly22descendants
  • K050272Cryomedical Instruments Cryo-Pac SystemsCryomedical Instruments, Ltd. · 2005 · 2 generations on11descendants
  • K100447Myoscience Cryo-TouchMyoscience, Inc. · 2010 · cites it directly10descendants
  • K142203Atricure Cryo Module System; cryoICE cryoablation probeAtriCure, Inc. · 2014 · 2 generations on9descendants
  • K102021Cryo-Touch IIMyoscience, Inc. · 2010 · 2 generations on9descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K831963Cryomedics NeurostatSpembly Medical, Ltd.1983—
+1K031482Cryostar System, Comprising: a) Cryostar Console, B) Cryostar 1MM Cryoprobe…Cryomedical Instruemts, Ltd.2003—
+2K050272Cryomedical Instruments Cryo-Pac SystemsCryomedical Instruments, Ltd.2005—
+1K100447Myoscience Cryo-TouchMyoscience, Inc.2010—
+2K142203Atricure Cryo Module System; cryoICE cryoablation probeAtriCure, Inc.2014—
+2K102021Cryo-Touch IIMyoscience, Inc.2010—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200310
200510
201020
201210
201310
201420
201510
201610
201710
201840
202010
202110
202210
202310
202420
202510
202610
FIG. 1 — Lineage of K831963, 1983–2026Source: FDA 510(k) summaries, read by 510(k) Report · 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 GXH? 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 GXH device

  1. #1 K250371 cryoICE cryoXT cryoablation probe (cryoXT)score 14.0 · 17 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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? (23)

See all 23

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K031482Cryostar System, Comprising: a) Cryostar Console, B) Cryostar 1MM Cryoprobe, C) Cryostar…Cryomedical Instruemts, Ltd.200322
K100447Myoscience Cryo-TouchMyoscience, Inc.201010

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?

  • Of its descendants, K031482 (Cryomedical Instruemts, Ltd., 2003) has gone furthest, with 22 descendants of its own.

How does its category compare?

All GXH devices

GXH Device, Surgical, Cryogenic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GXH

1in 2025

2010: 22012: 12013: 12014: 22015: 12017: 12018: 32020: 12021: 12022: 12023: 12024: 22025: 1
2007high 3 (2018) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GXH

52in 2018

2018: 52 days median
2007high 52 (2018)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GXH

No recall names GXH since 2007.

Adverse event reports per year · GXH

5in 2025

2015: 12016: 12017: 22018: 142019: 62020: 42021: 62022: 32023: 42024: 22025: 5
2007high 14 (2018) · low 0 (2007)2025

MAUDE reports naming product code GXH, 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
20090—00
20102—00
20110—00
20121—00
20131—00
20142—00
20151—01
20160—01
20171—02
2018352014
20190—06
20201—04
20211—06
20221—03
20231—04
20242—02
20251—05
20260—0—
Cite this page

510(k) Report. “K831963: Cryomedics Neurostat.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K831963

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