510(k) Report

510(k) · Cleared

Cleared

Surgical Stapling Instru., Auto, Suture

K771177510(k) TraditionalCleared Oct 18, 1977110-day reviewClass II21 CFR 878.4740

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

United States Surgical, A Division of Tyco Healthc · GAG Stapler, Surgical

Cleared on Oct 18, 1977 after a 110-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided
Oct 18, 1977
Review
110 days
Class
Class II
Product code
GAG
Recalls
None
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2009: 1 descendant cleared2012: 1 descendant cleared19801990200020102020
  1. This deviceK771177 Surgical Stapling Instru., Auto, SutureUnited States Surgical, A Division of Tyco Healthc · 1977
  2. Descendant · cites it directly · 1 of its ownK093253 Amid StaplerSafestitch, LLC · 2009
  3. Descendant · 2 generations on · 0 of its ownK120268 Amid StaplerSafestich Medical, LLC · 2012

Most influential descendants

Showing 2 of 2 · See all
  • K093253Amid StaplerSafestitch, LLC · 2009 · cites it directly1descendant
  • K120268Amid StaplerSafestich Medical, LLC · 2012 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K771177Surgical Stapling Instru., Auto, SutureUnited States Surgical, A Division of Tyco Healthc1977—
+1K093253Amid StaplerSafestitch, LLC2009—
+2K120268Amid StaplerSafestich Medical, LLC2012—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
201210
FIG. 1 — Lineage of K771177, 1977–2012Source: 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 GAG? 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 GAG device

  1. #1 K241629 ECHELON 3000 45mm Compact Stapler (ECH45C)…score 15.7 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 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? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K093253Amid StaplerSafestitch, LLC20091

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, K093253 (Safestitch, LLC, 2009) has gone furthest, with 1 descendant of its own.

How does its category compare?

All GAG devices

GAG Stapler, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GAG

2in 2025

2022: 12023: 42024: 32025: 22026 (partial year): 1
2007high 4 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GAG

138in 2024

2023: 102 days median2024: 138 days median
2007high 138 (2024) · low 102 (2023)2026

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

Recalls per year · GAG

1in 2018

2010: 12012: 12018: 1
2007high 1 (2010) · low 0 (2007)2026

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

Adverse event reports per year · GAG

1,065in 2025

2007: 9192008: 3662009: 182010: 222011: 192012: 492013: 1352014: 3022015: 1442016: 752017: 962018: 812019: 702020: 472021: 532022: 502023: 1092024: 1,1262025: 1,065
2007high 1,126 (2024) · low 18 (2009)2025

MAUDE reports naming product code GAG, 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—0919
20080—0366
20090—018
20100—122
20110—019
20120—149
20130—0135
20140—0302
20150—0144
20160—075
20170—096
20180—181
20190—070
20200—047
20210—053
20221—050
202341020109
2024313801,126
20252—01,065
20261—0—
Cite this page

510(k) Report. “K771177: Surgical Stapling Instru., Auto, Suture.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K771177

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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