510(k) Report

510(k) · Cleared

Recalled · 2007

Polypropylene, Nonabsorbable Surgical Sutures Usp

K001185510(k) TraditionalCleared Jun 23, 200073-day reviewClass II21 CFR 878.5010Recalls 1

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

Cp Medical · GAW Suture, Nonabsorbable, Synthetic, Polypropylene

Cleared on Jun 23, 2000 after a 73-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it. It has been recalled once.

Decided
Jun 23, 2000
Review
73 days
Class
Class II
Product code
GAW
Recalls
1
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2009: 1 descendant cleared200020052010201520202025
  1. This deviceK001185 Polypropylene, Nonabsorbable Surgical Sutures UspCp Medical · 2000
  2. Descendant · cites it directly · 0 of its ownK091574 Silk Black Braided Surgical Sutures, Nylon Monofilament Blue and…Supplidores Unidos Internacionales, S.A. · 2009

Most influential descendants

Showing 1 of 1 · See all
  • K091574Silk Black Braided Surgical Sutures, Nylon Monofilament Blue and Black Surgical SuturesSupplidores Unidos Internacionales, S.A. · 2009 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K001185Polypropylene, Nonabsorbable Surgical Sutures UspCp Medical2000—
+1K091574Silk Black Braided Surgical Sutures, Nylon Monofilament Blue and Black…Supplidores Unidos Internacionales, S.A.2009—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
FIG. 1 — Lineage of K001185, 2000–2009Source: 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 GAW? 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 GAW device

  1. #1 K253572 STRATAFIX™ Spiral PRONOVA™ Unidirectional…score 14.4 · 12 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? (1)

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

NumberDeviceApplicantDecidedDescendants
K091574Silk Black Braided Surgical Sutures, Nylon Monofilament Blue and Black Surgical SuturesSupplidores Unidos Internacionales, S.A.20090

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Apr 3, 2007Not classifiedZ-0808-2007OtherPotential for sterility of product to be compromised. Suture package seals incomplete or missing.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K091574 (Supplidores Unidos Internacionales, S.A., 2009) has gone furthest, with 0 descendants of its own.

How does its category compare?

All GAW devices

GAW Suture, Nonabsorbable, Synthetic, Polypropylene: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GAW

1in 2024

2007: 12010: 22012: 32013: 32014: 22015: 32016: 12017: 32018: 32019: 12020: 22022: 22023: 12024: 12026 (partial year): 1
2007high 3 (2012) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GAW

80in 2018

2012: 86 days median2013: 36 days median2015: 252 days median2017: 145 days median2018: 80 days median
2007high 252 (2015) · low 36 (2013)2026

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

Recalls per year · GAW

2so far in 2026, the most since 2007

2007: 12026 (partial year): 2
2007high 2 (2026) · low 0 (2008)2026

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

Adverse event reports per year · GAW

2,545in 2025

2007: 732008: 752009: 712010: 852011: 842012: 1942013: 1912014: 4372015: 4222016: 4402017: 4132018: 6852019: 1,8032020: 1,4932021: 1,6522022: 1,5632023: 1,8112024: 2,3482025: 2,545
2007high 2,545 (2025) · low 71 (2009)2025

MAUDE reports naming product code GAW, 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
20071—173
20080—075
20090—071
20102—085
20110—084
20123860194
20133360191
20142—0437
201532520422
20161—0440
201731450413
20183800685
20191—01,803
20202—01,493
20210—01,652
20222—01,563
20231—01,811
20241—02,348
20250—02,545
20261—2—
Cite this page

510(k) Report. “K001185: Polypropylene, Nonabsorbable Surgical Sutures Usp.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K001185

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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