510(k) Report

510(k) · Cleared

Recalled · Class II · 2022

SureForm 60 and SureForm 60 Reloads

K173721510(k) TraditionalCleared Jul 5, 2018212-day reviewClass II21 CFR 876.1500Recalls 3

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

Intuitive Surgical · NAY System, Surgical, Computer Controlled Instrument

Cleared on Jul 5, 2018 as substantially equivalent to K170508 (Intuitive Surgical, Inc., 2017) and 1 other predicate after a 212-day review. Its family tree reaches back 5 generations to 2005. 5 of the 20 devices in its family, counting itself, have a Class I recall. 6 later devices descend from it. It has been recalled 3 times.

Decided
Jul 5, 2018
Review
212 days
Class
Class II
Product code
NAY
Recalls
3
Predicates
2

Its longest line of descent runs back 5 generations to K051002 (2005). 13 ancestors in all, the oldest K033269 (2003). 6 later devices descend from it, 2 citing it directly. 5 of the 20 devices in this family, counting this one, have a Class I recall.

  1. Root · 5 generations backK051002 Endopath Endocutter 60 Endoscopic Linear CutterEthicon Endo-Surgery, Inc. · 2005 · Recalled
  2. 4 generations backK081146 Echelon Endoscopic Linear Cutters (Articulating and Straight)Ethicon Endo-Surgery, LLC · 2008 · Recalled (Class I)
  3. 3 generations backK112056 Echelon 60 Endoscopic Linear Cutter Reload, Black Model ECR60T…Ethicon Endo-Surgery, LLC · 2011 · Recalled
  4. 2 generations backK121600 Echelon 60 Endoscpic Linear Cutter Reload, WhiteEthicon Endo-Surgery, LLC · 2012
  5. 1 generation backK140560 Echelon Flex Powered Plus Articulating Endoscopic Linear Cutter…Ethicon Endo-Surgery, LLC · 2014 · Recalled (Class I)
  6. This deviceK173721 SureForm 60 and SureForm 60 ReloadsIntuitive Surgical · 2018
  7. Descendant · cites it directly · 5 of its ownK183224 SureForm 45, SureForm 45 ReloadsIntuitive Surgical · 2019 · Recalled
  8. Descendant · 2 generations on · 4 of its ownK190999 SureForm 45 Curved Tip, SureForm 45 Gray ReloadIntuitive Surgical, Inc. · 2019 · Recalled
  9. Descendant · 3 generations on · 2 of its ownK211997 8 mm SureForm 30 Curved-Tip Stapler, 8 mm SureForm 30 Stapler…Intuitive Surgical, Inc. · 2021 · Recalled (Class I)
  10. Descendant · cites it directly · 1 of its ownK222839 EndoWrist Stapler 30 System, EndoWrist Stapler 45 System, SureForm…Intuitive Surgical, Inc. · 2023 · Recalled (Class I)
  11. Descendant · 2 generations on · 0 of its ownK243596 da Vinci SP SureForm 45 Staplers and Reloads (SP1098)Intuitive Surgical, Inc. · 2025

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2019: 22021: 12023: 12024: 12025: 1
2019high 2 (2019) · low 0 (2020)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 6 · See all
  • K183224SureForm 45, SureForm 45 ReloadsIntuitive Surgical · 2019 · cites it directly5descendants
  • K190999SureForm 45 Curved Tip, SureForm 45 Gray ReloadIntuitive Surgical, Inc. · 2019 · 2 generations on4descendants
  • K2119978 mm SureForm 30 Curved-Tip Stapler, 8 mm SureForm 30 Stapler, SureForm 30 ReloadsIntuitive Surgical, Inc. · 2021 · 3 generations on2descendants
  • K222839EndoWrist Stapler 30 System, EndoWrist Stapler 45 System, SureForm 45 System, SureForm…Intuitive Surgical, Inc. · 2023 · cites it directly1descendant
  • K243596da Vinci SP SureForm 45 Staplers and Reloads (SP1098)Intuitive Surgical, Inc. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K051002Endopath Endocutter 60 Endoscopic Linear CutterEthicon Endo-Surgery, Inc.20051
−4K081146Echelon Endoscopic Linear Cutters (Articulating and Straight)Ethicon Endo-Surgery, LLC2008Class I
−3K112056Echelon 60 Endoscopic Linear Cutter Reload, Black Model ECR60T, Echelon 45…Ethicon Endo-Surgery, LLC20111
−2K121600Echelon 60 Endoscpic Linear Cutter Reload, WhiteEthicon Endo-Surgery, LLC2012—
−1K140560Echelon Flex Powered Plus Articulating Endoscopic Linear Cutter, 60MM…Ethicon Endo-Surgery, LLC2014Class I
0 (this device)K173721SureForm 60 and SureForm 60 ReloadsIntuitive Surgical2018—
+1K183224SureForm 45, SureForm 45 ReloadsIntuitive Surgical20191
+2K190999SureForm 45 Curved Tip, SureForm 45 Gray ReloadIntuitive Surgical, Inc.20191
+3K2119978 mm SureForm 30 Curved-Tip Stapler, 8 mm SureForm 30 Stapler, SureForm 30…Intuitive Surgical, Inc.2021Class I
+1K222839EndoWrist Stapler 30 System, EndoWrist Stapler 45 System, SureForm 45 System…Intuitive Surgical, Inc.2023Class I
+2K243596da Vinci SP SureForm 45 Staplers and Reloads (SP1098)Intuitive Surgical, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200310
200710
201110
201320
201410
201610
201710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201920
202111
202311
202411
202510
FIG. 1 — Lineage of K173721, 2005–2025Source: 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), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

5 devices in this family have a Class I recall. 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 NAY device

  1. #1 K232610 da Vinci Surgical System Model IS5000, da…score 32.9 · 24 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? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K170508EndoWrist Stapler 45 Instrument, EndoWrist Stapler 45 Reloads, EndoWrist Stapler 30…
Summary page 4
…General and Plastic Surgery Predicate Device: 1. Primary: IS4000 EndoWrist® Stapler 45 and Stapler 45 Reloads – K170508 2. Secondary: Echelon Flex 60 Powered Plus Articulating Endoscopic Lin…
Intuitive Surgical, Inc.2017—
*K140560Echelon Flex Powered Plus Articulating Endoscopic Linear Cutter, 60MM, Standard, Echelon…
Summary page 4
…Endoscopic Linear Cutter, Echelon 60 mm Endoscopic Linear Cutter Reload, PSEE60A (Stapler) GST60X (Reloads) - K140560 Device Description: The Intuitive Surgical SureForm 60 and SureForm 60 Reloads is a disposable surgical stapler system designe…
Ethicon Endo-Surgery, LLC2014Class I
†K053202Gore Seamguard Bioabsorbable Staple Line Reinforcement MaterialW.L. Gore & Associates2005—
†K170945Biodesign Staple Line ReinforcementCook Biotech Incorporated2017—

Also cleared against K170508: 3 other devices →

What descends from it? (6)

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

NumberDeviceApplicantDecidedDescendants
K183224SureForm 45, SureForm 45 ReloadsIntuitive Surgical20195
K222839EndoWrist Stapler 30 System, EndoWrist Stapler 45 System, SureForm 45 System, SureForm… Class IIntuitive Surgical, Inc.20231

Has anything in its family been recalled? (5 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Mar 17, 2022Class IIZ-0999-2022Under Investigation by firmAs a result of complaint data review, it identified tissue pushout events occurring during firing of the SureForm stapler when tissue is pushed distally within the jaws, rather than being held in place and transected. Overall rate of harm…
Jul 1, 2019Class IIZ-1890-2020Employee errorThe firm became aware of a manufacturing variation in which black and green reloads in select Stapler Reloads may not deploy individual adjacent staples, which could result in an incomplete staple line. Failure of a incomplete staple like…
Jul 1, 2019Class IIZ-1891-2020Employee errorThe firm became aware of a manufacturing variation in which black and green reloads in select Stapler Reloads may not deploy individual adjacent staples, which could result in an incomplete staple line. Failure of a incomplete staple like…

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K140560Echelon Flex Powered Plus Articulating Endoscopic Linear Cutter, 60MM, Standard, Echelon Flex Powered Plus…Ethicon Endo-Surgery, LLC · 2014 · Direct predicate · ◆ on the line of descent in FIG. 12 Class I recalls
  • K081146Echelon Endoscopic Linear Cutters (Articulating and Straight)Ethicon Endo-Surgery, LLC · 2008 · 3 generations back · ◆ on the line of descent in FIG. 11 Class I recall
  • K222839EndoWrist Stapler 30 System, EndoWrist Stapler 45 System, SureForm 45 System, SureForm 60 System, 8 mm…Intuitive Surgical, Inc. · 2023 · Cites it directly · ◆ in the 2023 descendants bar of FIG. 11 Class I recall
  • K2416388mm SureForm 30 Curved-Tip Stapler; 8mm SureForm 30 Stapler; 8mm SureForm 30 ReloadsIntuitive Surgical, Inc. · 2024 · 2 generations on · ◆ in the 2024 descendants bar of FIG. 11 Class I recall
  • K2119978 mm SureForm 30 Curved-Tip Stapler, 8 mm SureForm 30 Stapler, SureForm 30 ReloadsIntuitive Surgical, Inc. · 2021 · 3 generations on · ◆ in the 2021 descendants bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 13 years and passes through 3 companies; a new generation was cleared every 3.1 years on median.
  • 7 of the 13 ancestors have a recall of any class; 2 have a Class I recall.
  • Of its descendants, K183224 (Intuitive Surgical, 2019) has gone furthest, with 5 descendants of its own.
  • 3 other devices also cite its predicate K170508.

How does its category compare?

All NAY devices

NAY System, Surgical, Computer Controlled Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · NAY

16in 2025

2008: 42009: 32010: 12011: 72012: 42013: 42014: 92015: 32016: 82017: 162018: 152019: 82020: 92021: 112022: 62023: 52024: 102025: 162026 (partial year): 7
2007high 16 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NAY

117in 2025

2008: 189 days median2009: 253 days median2011: 191 days median2012: 106 days median2013: 144 days median2014: 143 days median2015: 99 days median2016: 197 days median2017: 107 days median2018: 152 days median2019: 73 days median2020: 212 days median2021: 61 days median2022: 57 days median2023: 141 days median2024: 126 days median2025: 117 days median2026 (partial year): 89 days median
2007high 253 (2009) · low 57 (2022)2026

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

Recalls per year · NAY

1in 2025

2007: 112008: 32009: 12011: 22012: 12013: 62014: 252015: 32016: 12017: 12018: 22019: 52021: 32022: 32023: 2, 1 Class I2024: 402025: 12026 (partial year): 4, 1 Class I
2007high 40 (2024) · low 0 (2010)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · NAY

48,456in 2025

2007: 1332008: 2242009: 3802010: 6232011: 5012012: 1,5522013: 6,2172014: 6,1352015: 1,7222016: 1,0772017: 1,0492018: 1,0742019: 1,1542020: 1,5582021: 1,9972022: 5,7272023: 10,8982024: 12,8722025: 48,456
2007high 48,456 (2025) · low 133 (2007)2025

MAUDE reports naming product code NAY, 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—11133
200841893224
200932531380
20101—0623
201171912501
2012410611,552
2013414466,217
20149143256,135
201539931,722
2016819711,077
20171610711,049
20181515221,074
201987351,154
2020921201,558
2021116131,997
202265735,727
202351412 (1)10,898
2024101264012,872
202516117148,456
20267894 (1)—

What is it indicated for?

The Intuitive Surgical Stapler SureForm 60, Stapler SureForm 60 reloads, and other stapler accessories are intended to be used with a compatible da Vinci Surgical Systems for resection, transection, and, or creation of anastomoses in General, Thoracic, Gynecologic, Urologic, and Pediatric surgery. The device can be used with staple line or tissue buttressing material (natural or synthetic).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K173721: SureForm 60 and SureForm 60 Reloads.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K173721

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026