510(k) · Cleared
Recalled · Class II · 2024Surgisis RVP Recto-Vaginal Fistula Plug
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Cook Biotech, Inc. · FTM Mesh, Surgical
Cleared on Oct 10, 2006 as substantially equivalent to K050337 (Cook Biotech, Inc., 2005) after a 27-day review. Its family tree reaches back 5 generations to 1992. It has been recalled 12 times.
- Decided
- Oct 10, 2006
- Review
- 27 days
- Class
- Class II
- Product code
- FTM
- Recalls
- 12
- Predicates
- 1
Its longest line of descent runs back 5 generations to K921895 (1992). 11 ancestors in all, the oldest K830889 (1983). No later device cites it as a predicate yet.
- Root · 5 generations backK921895 Tissue Patch, Tissue GraftBio-Vascular, Inc. · 1992
- 4 generations backK961810 Supple Peri-Guard PericardiumBio-Vascular, Inc. · 1996
- 3 generations backK980431 SurgisisCook Biotech, Inc. · 1998
- 2 generations backK992159 Surgisis SlingCook Biotech, Inc. · 1999
- 1 generation backK050337 Sis Fistula PlugCook Biotech, Inc. · 2005
- This deviceK062729 Surgisis RVP Recto-Vaginal Fistula PlugCook Biotech, Inc. · 2006
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K921895 | Tissue Patch, Tissue Graft | Bio-Vascular, Inc. | 1992 | — |
| −4 | K961810 | Supple Peri-Guard Pericardium | Bio-Vascular, Inc. | 1996 | — |
| −3 | K980431 | Surgisis | Cook Biotech, Inc. | 1998 | — |
| −2 | K992159 | Surgisis Sling | Cook Biotech, Inc. | 1999 | — |
| −1 | K050337 | Sis Fistula Plug | Cook Biotech, Inc. | 2005 | — |
| 0 (this device) | K062729 | Surgisis RVP Recto-Vaginal Fistula Plug | Cook Biotech, Inc. | 2006 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1983 | 1 | 0 |
| 1992 | 1 | 0 |
| 1996 | 2 | 0 |
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
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.
Planning a device in FTM? 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 FTM device
- #1 K262406 EluPro Antibiotic-Eluting BioEnvelopescore 15.1 · 12 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K050337 | Sis Fistula PlugSummary page 1…21 CER 878.3300 (FTMI) Class II Predicate Device: The predicate device is the original SIS Fistula Plug [5 10(k) No. K050337], cleared for marketing by the Food and Drug Administration on March 9, 2005. Device Description:… | 2005 |
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
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Aug 7, 2024 | Class II | Z-3260-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3261-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3254-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3252-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3251-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3256-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3255-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3259-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3257-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3258-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3253-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
| Aug 7, 2024 | Class II | Z-3250-2024 | Incorrect or no expiration date | Products expire prior to the expiration date printed on the product labeling |
The 5 latest of 12 recalls; the web page lists all.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 14 years and passes through 2 companies; a new generation was cleared every 2.0 years on median.
- None of the 11 ancestors has a recall.
- 7 other devices also cite its predicate K050337.
How does its category compare?
All FTM devicesFTM Mesh, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · FTM
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FTM
29in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FTM
1in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FTM
232in 2025
MAUDE reports naming product code FTM, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 9 | 104 | 7 | 60 |
| 2008 | 9 | 86 | 1 | 141 |
| 2009 | 7 | 86 | 0 | 476 |
| 2010 | 2 | — | 1 | 197 |
| 2011 | 6 | 100 | 8 | 288 |
| 2012 | 4 | 66 | 0 | 467 |
| 2013 | 4 | 123 | 0 | 3,351 |
| 2014 | 8 | 153 | 0 | 1,093 |
| 2015 | 4 | 316 | 0 | 977 |
| 2016 | 7 | 88 | 0 | 509 |
| 2017 | 9 | 147 | 0 | 529 |
| 2018 | 2 | — | 21 | 357 |
| 2019 | 6 | 107 | 4 | 418 |
| 2020 | 4 | 59 | 1 | 457 |
| 2021 | 4 | 61 | 1 | 369 |
| 2022 | 0 | — | 0 | 375 |
| 2023 | 2 | — | 1 | 485 |
| 2024 | 3 | 29 | 0 | 383 |
| 2025 | 1 | — | 0 | 232 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The modified SIS Fistula Plug is for implantation to reinforce soft tissue for repair of recto-vaginal fistulas. The device is supplied sterile and is intended for one-time use.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K062729 · printed Nov 4, 2026
Cite this page
510(k) Report. “K062729: Surgisis RVP Recto-Vaginal Fistula Plug.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K062729
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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