510(k) Report

510(k) · Cleared

Cleared

Apogee and Perigee Systems with Intepro Lite and Intexen LP, Part of the Ams; Pelvic Floor Repair System

K082387510(k) SpecialCleared Dec 4, 2008107-day reviewClass III21 CFR 884.5980

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

American Medical Systems · OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed

Cleared on Dec 4, 2008 as substantially equivalent to K051485 (American Medical Systems, Inc., 2005) after a 107-day review. Its family tree reaches back 11 generations to 1993.

Decided
Dec 4, 2008
Review
107 days
Class
Class III
Product code
OTP
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K931386 (1993). 39 ancestors in all, the oldest K830889 (1983). No later device cites it as a predicate yet.

  1. Root · 11 generations backK931386 Hemashield Microvel/Woven Double Velour FabricMeadox Medicals, Div. Boston Scientific Corp. · 1993
  2. 7 generations between
  3. 3 generations backK040623 Ams Perigee SystemAmerican Medical Systems, Inc. · 2004
  4. 2 generations backK050445 Ams Collagen Dermal MatrixAmerican Medical Systems, Inc. · 2005 · Recalled
  5. 1 generation backK051485 Ams Pelvic Floor Repair SystemAmerican Medical Systems, Inc. · 2005
  6. This deviceK082387 Apogee and Perigee Systems with Intepro Lite and Intexen LP, Part of…American Medical Systems · 2008
Show all 11 generations
  1. Root · 11 generations backK931386 Hemashield Microvel/Woven Double Velour FabricMeadox Medicals, Div. Boston Scientific Corp. · 1993
  2. 10 generations backK963611 Vascutek Cardiovascular Fabric: Vascutek Gelseal Patch,Vascutek…Vascutek, Ltd. · 1996 · Recalled
  3. 9 generations backK972651 IN-SlingInfluence, Inc. · 1997
  4. 8 generations backK980482 Triangle SlingInfluence, Inc. · 1998
  5. 7 generations backK002721 Ams Triangle Silicone-Coated Sling and Surgical MeshAmerican Medical Systems, Inc. · 2000
  6. 6 generations backK010931 Ams Sacral Colpopexy Sling, Model 72403501American Medical Systems, Inc. · 2001
  7. 5 generations backK033636 Ams Large Pore Polypropylene MeshAmerican Medical Systems, Inc. · 2003
  8. 4 generations backK040521 Modification to Ams Large Pore Polypropylene MeshAmerican Medical Systems, Inc. · 2004
  9. 3 generations backK040623 Ams Perigee SystemAmerican Medical Systems, Inc. · 2004
  10. 2 generations backK050445 Ams Collagen Dermal MatrixAmerican Medical Systems, Inc. · 2005 · Recalled
  11. 1 generation backK051485 Ams Pelvic Floor Repair SystemAmerican Medical Systems, Inc. · 2005
  12. This deviceK082387 Apogee and Perigee Systems with Intepro Lite and Intexen LP, Part of…American Medical Systems · 2008
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K931386Hemashield Microvel/Woven Double Velour FabricMeadox Medicals, Div. Boston Scientific Corp.1993—
−10K963611Vascutek Cardiovascular Fabric: Vascutek Gelseal Patch,Vascutek Gelsoft…Vascutek, Ltd.19961
−9K972651IN-SlingInfluence, Inc.1997—
−8K980482Triangle SlingInfluence, Inc.1998—
−7K002721Ams Triangle Silicone-Coated Sling and Surgical MeshAmerican Medical Systems, Inc.2000—
−6K010931Ams Sacral Colpopexy Sling, Model 72403501American Medical Systems, Inc.2001—
−5K033636Ams Large Pore Polypropylene MeshAmerican Medical Systems, Inc.2003—
−4K040521Modification to Ams Large Pore Polypropylene MeshAmerican Medical Systems, Inc.2004—
−3K040623Ams Perigee SystemAmerican Medical Systems, Inc.2004—
−2K050445Ams Collagen Dermal MatrixAmerican Medical Systems, Inc.20051
−1K051485Ams Pelvic Floor Repair SystemAmerican Medical Systems, Inc.2005—
0 (this device)K082387Apogee and Perigee Systems with Intepro Lite and Intexen LP, Part of the Ams…American Medical Systems2008—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198310
199230
199640
199710
199830
199920
200020
200130
200250
200310
200430
FIG. 1 — Lineage of K082387, 1993–2008Source: 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.

Planning a device in OTP? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K051485Ams Pelvic Floor Repair System
Summary page 1
…Class II, 21 CFR Part 878.3300 Classification Name: Surgical Mesh, polymeric (OTP) PAT) Predicate Device: Apogee and Perigee Systems with IntePro Lite and InteXen LP (K051485), Part of the AMS Pelvic Floor Repair System , lndlcétlons for Use AMS Pelvic Floor Repair System is intended for use where the…
American Medical Systems, Inc.2005—

Also cleared against K051485: 4 other devices →

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.

What does this lineage say?

  • The line of descent spans 15 years and passes through 5 companies; a new generation was cleared every 10 months on median.
  • 4 of the 39 ancestors have a recall of any class.
  • 4 other devices also cite its predicate K051485.

How does its category compare?

All OTP devices

OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · OTP

2in 2012

2007: 42008: 82009: 62011: 52012: 2
2007high 8 (2008) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OTP

71in 2011

2007: 90 days median2008: 103 days median2009: 21 days median2011: 71 days median
2007high 103 (2008) · low 21 (2009)2026

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

Recalls per year · OTP

No recall names OTP since 2007.

Adverse event reports per year · OTP

26in 2025

2007: 12009: 32010: 32011: 322012: 4942013: 7,1502014: 7782015: 6842016: 4152017: 2732018: 3922019: 3682020: 1752021: 6472022: 1142023: 592024: 352025: 26
2007high 7,150 (2013) · low 0 (2008)2025

MAUDE reports naming product code OTP, 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
200749001
2008810300
200962103
20100—03
2011571032
20122—0494
20130—07,150
20140—0778
20150—0684
20160—0415
20170—0273
20180—0392
20190—0368
20200—0175
20210—0647
20220—0114
20230—059
20240—035
20250—026
20260—0—

What is it indicated for?

AMS Pelvic Floor Repair System is intended for use where the connective tissue has ruptured or for implantation to reinforce soft tissues where weakness exists in the urological, gynecological and gastroenterological anatomy, This includes but is not limited to the following procedures: pubourethral support, including urethral slings for the treatment of incontinence, vaginal wall prolapse repairs including anterior and posterior wall repairs, vaginal suspension, reconstruction of the pelvic floor and tissue repair.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K082387: Apogee and Perigee Systems with Intepro Lite and Intexen LP, Part of the Ams; Pelvic Floor Repair System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K082387

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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