510(k) Report

510(k) · Cleared

Cleared

Stryker Self-Punching ICONIX

K172921510(k) TraditionalCleared Nov 20, 201756-day reviewClass II21 CFR 888.3040

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

Stryker · MBI Fastener, Fixation, Nondegradable, Soft Tissue

Cleared on Nov 20, 2017 as substantially equivalent to K171465 (Stryker, 2017) after a 56-day review. Its family tree reaches back 13 generations to 1991.

Decided
Nov 20, 2017
Review
56 days
Class
Class II
Product code
MBI
Recalls
None
Predicates
1

Its longest line of descent runs back 13 generations to K911837 (1991). 99 ancestors in all, the oldest K792022 (1979). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2014: 1 other ancestor2012: 1 other ancestor2011: 3 other ancestors2007: 5 other ancestors2001: 5 other ancestors2009: 1 other ancestor2006: 3 other ancestors2005: 3 other ancestors2004: 2 other ancestors2000: 4 other ancestors1997: 12 other ancestors2008: 1 other ancestor2002: 2 other ancestors1999: 5 other ancestors1996: 13 other ancestors2003: 1 other ancestor1998: 7 other ancestors1995: 8 other ancestors1990: 1 other ancestor1982: 1 other ancestor1994: 2 other ancestors1993: 1 other ancestor1992: 3 other ancestors1979: 1 other ancestorReference device: K162310 · XBraid TT Suture Tape · Stryker · 2016K911837 · Suretac Polyglyconate Absorbable Fixation Device · Acufex Microsurgical, Inc. · 1991K973849 · Bioabsorbable Bankart Tack · Hogan & Hartson · 1998K992567 · Anatomical Bankart Tack, Model 523520A · Bionx Implants, Ltd. · 1999K003970 · Contour Labral Nail, Model 533520A · Bionx Implants, Inc. · 2001K020056 · Duet Suture Anchor · Bionx Implants, Ltd. · 2002K030388 · Impact Suture Anchor. Model 433510 · Bionx Implants, Ltd. · 2003K042966 · Duet Suture Anchor, Models BXS4216, BXS4216H; Impact Suture Anchor, Models BXS4218, BXS4218H · Linvatec Biomaterials, Ltd. · 2004K053561 · Bio-Mini Revo Suture Anchor · Conmed Linvatec · 2006K091549 · Conmed Linvatec Soft Tissue to Bone System · Linvatec Corp. · 2009 · recalledK111779 · Y-Knot All-Suture Anchor Model HF13 · Conmed Linvatec · 2011K131035 · Y-Knot Flex All-Suture Anchor, W/ Two #2 (5 Metric) HI-FI Sutures, 1.8MM · Linvatec Corporation D/B/A Conmed Linvatec · 2013K133224 · Y-Knot RC All-Suture Anchor, 2.8MM - Double Loaded and Triple Loaded W/ #2 Hifi Sutures · Conmed Corporation · 2014K171465 · Stryker Self-Punching ICONIX · Stryker · 20171980199020002010
Other ancestors, by generation 2 generations back: 1 other ancestor3 generations back: 2 other ancestors4 generations back: 4 other ancestors5 generations back: 10 other ancestors6 generations back: 11 other ancestors7 generations back: 31 other ancestors8 generations back: 21 other ancestors9 generations back: 6 other ancestors K171465 · Stryker Self-Punching ICONIX · Stryker · 2017K133224 · Y-Knot RC All-Suture Anchor, 2.8MM - Double Loaded and Triple Loaded W/ #2 Hifi Sutures · Conmed Corporation · 2014K131035 · Y-Knot Flex All-Suture Anchor, W/ Two #2 (5 Metric) HI-FI Sutures, 1.8MM · Linvatec Corporation D/B/A Conmed Linvatec · 2013K111779 · Y-Knot All-Suture Anchor Model HF13 · Conmed Linvatec · 2011K091549 · Conmed Linvatec Soft Tissue to Bone System · Linvatec Corp. · 2009 · recalledK053561 · Bio-Mini Revo Suture Anchor · Conmed Linvatec · 2006K042966 · Duet Suture Anchor, Models BXS4216, BXS4216H; Impact Suture Anchor, Models BXS4218, BXS4218H · Linvatec Biomaterials, Ltd. · 2004K030388 · Impact Suture Anchor. Model 433510 · Bionx Implants, Ltd. · 2003K020056 · Duet Suture Anchor · Bionx Implants, Ltd. · 2002K003970 · Contour Labral Nail, Model 533520A · Bionx Implants, Inc. · 2001K992567 · Anatomical Bankart Tack, Model 523520A · Bionx Implants, Ltd. · 1999K973849 · Bioabsorbable Bankart Tack · Hogan & Hartson · 1998K911837 · Suretac Polyglyconate Absorbable Fixation Device · Acufex Microsurgical, Inc. · 1991−10−50
  1. Root · 13 generations backK911837 Suretac Polyglyconate Absorbable Fixation DeviceAcufex Microsurgical, Inc. · 1991
  2. 9 generations between
  3. 3 generations backK131035 Y-Knot Flex All-Suture Anchor, W/ Two #2 (5 Metric) HI-FI Sutures…Linvatec Corporation D/B/A Conmed Linvatec · 2013
  4. 2 generations backK133224 Y-Knot RC All-Suture Anchor, 2.8MM - Double Loaded and Triple Loaded…Conmed Corporation · 2014
  5. 1 generation backK171465 Stryker Self-Punching ICONIXStryker · 2017
  6. This deviceK172921 Stryker Self-Punching ICONIXStryker · 2017
Show all 13 generations
  1. Root · 13 generations backK911837 Suretac Polyglyconate Absorbable Fixation DeviceAcufex Microsurgical, Inc. · 1991
  2. 12 generations backK973849 Bioabsorbable Bankart TackHogan & Hartson · 1998
  3. 11 generations backK992567 Anatomical Bankart Tack, Model 523520ABionx Implants, Ltd. · 1999
  4. 10 generations backK003970 Contour Labral Nail, Model 533520ABionx Implants, Inc. · 2001
  5. 9 generations backK020056 Duet Suture AnchorBionx Implants, Ltd. · 2002
  6. 8 generations backK030388 Impact Suture Anchor. Model 433510Bionx Implants, Ltd. · 2003
  7. 7 generations backK042966 Duet Suture Anchor, Models BXS4216, BXS4216H; Impact Suture Anchor…Linvatec Biomaterials, Ltd. · 2004
  8. 6 generations backK053561 Bio-Mini Revo Suture AnchorConmed Linvatec · 2006
  9. 5 generations backK091549 Conmed Linvatec Soft Tissue to Bone SystemLinvatec Corp. · 2009 · Recalled
  10. 4 generations backK111779 Y-Knot All-Suture Anchor Model HF13Conmed Linvatec · 2011
  11. 3 generations backK131035 Y-Knot Flex All-Suture Anchor, W/ Two #2 (5 Metric) HI-FI Sutures…Linvatec Corporation D/B/A Conmed Linvatec · 2013
  12. 2 generations backK133224 Y-Knot RC All-Suture Anchor, 2.8MM - Double Loaded and Triple Loaded…Conmed Corporation · 2014
  13. 1 generation backK171465 Stryker Self-Punching ICONIXStryker · 2017
  14. This deviceK172921 Stryker Self-Punching ICONIXStryker · 2017
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K911837Suretac Polyglyconate Absorbable Fixation DeviceAcufex Microsurgical, Inc.1991—
−12K973849Bioabsorbable Bankart TackHogan & Hartson1998—
−11K992567Anatomical Bankart Tack, Model 523520ABionx Implants, Ltd.1999—
−10K003970Contour Labral Nail, Model 533520ABionx Implants, Inc.2001—
−9K020056Duet Suture AnchorBionx Implants, Ltd.2002—
−8K030388Impact Suture Anchor. Model 433510Bionx Implants, Ltd.2003—
−7K042966Duet Suture Anchor, Models BXS4216, BXS4216H; Impact Suture Anchor, Models…Linvatec Biomaterials, Ltd.2004—
−6K053561Bio-Mini Revo Suture AnchorConmed Linvatec2006—
−5K091549Conmed Linvatec Soft Tissue to Bone SystemLinvatec Corp.20091
−4K111779Y-Knot All-Suture Anchor Model HF13Conmed Linvatec2011—
−3K131035Y-Knot Flex All-Suture Anchor, W/ Two #2 (5 Metric) HI-FI Sutures, 1.8MMLinvatec Corporation D/B/A Conmed Linvatec2013—
−2K133224Y-Knot RC All-Suture Anchor, 2.8MM - Double Loaded and Triple Loaded W/ #2…Conmed Corporation2014—
−1K171465Stryker Self-Punching ICONIXStryker2017—
0 (this device)K172921Stryker Self-Punching ICONIXStryker2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198210
199010
199230
199310
199420
199580
1996130
1997120
199870
199950
200040
200150
200220
200310
200420
200530
200630
200750
200810
200910
201130
201210
201410
FIG. 1 — Lineage of K172921, 1991–2017Source: 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 MBI? 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 MBI device

  1. #1 K203268 Arthrex FiberTak Suture Anchorscore 21.4 · 11 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? (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
*K171465Stryker Self-Punching ICONIX
Summary page 4
…II Product Code: MBI III. PREDICATE AND REFERENCE DEVICE Predicate Device: Device Name: Stryker Self-Punching ICONIX Company Name: Stryker 510(k) #: K171465 Reference Device: Device Name: XBraid TT Suture Tape Company Name: Stryker 510(k) #: K162310 Predicate and reference devices ha…
Stryker2017—
†K162310XBraid TT Suture TapeStryker2016—

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 26 years and passes through 10 companies; a new generation was cleared every 1.6 years on median.
  • 9 of the 99 ancestors have a recall of any class.

How does its category compare?

All MBI devices

MBI Fastener, Fixation, Nondegradable, Soft Tissue: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · MBI

27in 2025

2007: 162008: 102009: 192010: 172011: 302012: 242013: 312014: 232015: 232016: 172017: 172018: 162019: 312020: 352021: 182022: 192023: 522024: 222025: 272026 (partial year): 30
2007high 52 (2023) · low 10 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MBI

58in 2025

2007: 80 days median2008: 69 days median2009: 82 days median2010: 76 days median2011: 75 days median2012: 94 days median2013: 100 days median2014: 101 days median2015: 85 days median2016: 94 days median2017: 70 days median2018: 91 days median2019: 90 days median2020: 83 days median2021: 107 days median2022: 64 days median2023: 57 days median2024: 30 days median2025: 58 days median2026 (partial year): 63 days median
2007high 107 (2021) · low 30 (2024)2026

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

Recalls per year · MBI

1in 2025

2007: 242008: 62009: 22010: 32011: 232012: 62013: 22017: 42018: 22020: 12023: 12024: 12025: 1
2007high 24 (2007) · low 0 (2014)2026

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

Adverse event reports per year · MBI

3,826in 2025

2007: 2402008: 3382009: 3552010: 2912011: 3282012: 3712013: 4422014: 5042015: 5072016: 7952017: 6752018: 1,0722019: 1,3032020: 1,4542021: 1,8902022: 1,5912023: 2,5032024: 3,7792025: 3,826
2007high 3,826 (2025) · low 240 (2007)2025

MAUDE reports naming product code MBI, 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
2007168024240
200810696338
200919822355
201017763291
2011307523328
201224946371
2013311002442
2014231010504
201523850507
201617940795
201717704675
2018169121,072
2019319001,303
2020358311,454
20211810701,890
2022196401,591
2023525712,503
2024223013,779
2025275813,826
202630630—

What is it indicated for?

The Stryker Self-Punching ICONIX Anchors are intended to be used for soft-tissue to bone fixation in the shoulder.

They are indicated for use in rotator cuff 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. “K172921: Stryker Self-Punching ICONIX.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K172921

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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