510(k) Report

510(k) · Cleared

Cleared

Rog Suture Anchor, Rog Knotless Suture Anchor

K111590510(k) SpecialCleared Aug 8, 201162-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

Rog Sports Medicine, Inc. · MBI Fastener, Fixation, Nondegradable, Soft Tissue

Cleared on Aug 8, 2011 as substantially equivalent to K110229 (Rog Sports Medicine, Inc., 2011) and 1 other predicate after a 62-day review. Its family tree reaches back 5 generations to 1996. 5 later devices descend from it.

Decided
Aug 8, 2011
Review
62 days
Class
Class II
Product code
MBI
Recalls
None
Predicates
2

Its longest line of descent runs back 5 generations to K961555 (1996). 25 ancestors in all, the oldest K931519 (1994). 5 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2011: 1 other ancestor2007: 2 other ancestors2006: 2 other ancestors2004: 2 other ancestors2001: 5 other ancestors2002: 1 other ancestor1998: 3 other ancestors1995: 2 other ancestors1994: 1 other ancestor1996: 1 other ancestor2023: 1 descendant cleared2011: 2 descendants cleared2020: 1 descendant cleared2018: 1 descendant clearedK961555 · Acufex Tag Bioabsorbable Anchors · Acufex Microsurgical, Inc. · 1996K031685 · Tag Rod Bioraptor Suture Anchor 7209317, 7209318 · Smith & Nephew, Inc. · 2003 · recalledK053344 · Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture Anchor · Smith & Nephew, Inc. · 2006K061863 · Arthrex Corkscrew Suture Anchor, Tak, and Pushlock Family · Arthrex, Inc. · 2006K110229 · Rog Suture Anchor 5.5MM, 2.9MM · Rog Sports Medicine, Inc. · 20111990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 3 other ancestors3 generations back: 4 other ancestors4 generations back: 9 other ancestors5 generations back: 3 other ancestors 1 generation forward: 4 descendants2 generations forward: 1 descendant K110229 · Rog Suture Anchor 5.5MM, 2.9MM · Rog Sports Medicine, Inc. · 2011K061863 · Arthrex Corkscrew Suture Anchor, Tak, and Pushlock Family · Arthrex, Inc. · 2006K053344 · Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture Anchor · Smith & Nephew, Inc. · 2006K031685 · Tag Rod Bioraptor Suture Anchor 7209317, 7209318 · Smith & Nephew, Inc. · 2003 · recalledK961555 · Acufex Tag Bioabsorbable Anchors · Acufex Microsurgical, Inc. · 1996−50
  1. Root · 5 generations backK961555 Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc. · 1996
  2. 4 generations backK031685 Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc. · 2003 · Recalled
  3. 3 generations backK053344 Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5…Smith & Nephew, Inc. · 2006
  4. 2 generations backK061863 Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc. · 2006
  5. 1 generation backK110229 Rog Suture Anchor 5.5MM, 2.9MMRog Sports Medicine, Inc. · 2011
  6. This deviceK111590 Rog Suture Anchor, Rog Knotless Suture AnchorRog Sports Medicine, Inc. · 2011
  7. Descendant · cites it directly · 2 of its ownK113299 Rog Suture AnchorRog Sports Medicine, Inc. · 2011
  8. Descendant · cites it directly · 1 of its ownK112991 Modified Rog Suture AnchorRog Sports Medicine, Inc. · 2011
  9. Descendant · cites it directly · 0 of its ownK230517 Legends Orthopedics Suture Anchors (Legends Orthopedics 5.5 mm…Jarmon Medical, LLC (Dba Legends Orthopedics) · 2023
  10. Descendant · cites it directly · 0 of its ownK192949 Flower Suture Anchor SetFlower Orthopedics Corporation · 2020
  11. Descendant · 2 generations on · 0 of its ownK182736 OIC Suture Anchor SystemThe Orthopaedic Implant Company · 2018

Most influential descendants

Showing 5 of 5 · See all
  • K113299Rog Suture AnchorRog Sports Medicine, Inc. · 2011 · cites it directly2descendants
  • K112991Modified Rog Suture AnchorRog Sports Medicine, Inc. · 2011 · cites it directly1descendant
  • K230517Legends Orthopedics Suture Anchors (Legends Orthopedics 5.5 mm Suture Anchors, Legends…Jarmon Medical, LLC (Dba Legends Orthopedics) · 2023 · cites it directly0descendants
  • K192949Flower Suture Anchor SetFlower Orthopedics Corporation · 2020 · cites it directly0descendants
  • K182736OIC Suture Anchor SystemThe Orthopaedic Implant Company · 2018 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K961555Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc.1996—
−4K031685Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc.20035
−3K053344Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture…Smith & Nephew, Inc.2006—
−2K061863Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc.2006—
−1K110229Rog Suture Anchor 5.5MM, 2.9MMRog Sports Medicine, Inc.2011—
0 (this device)K111590Rog Suture Anchor, Rog Knotless Suture AnchorRog Sports Medicine, Inc.2011—
+1K113299Rog Suture AnchorRog Sports Medicine, Inc.2011—
+1K112991Modified Rog Suture AnchorRog Sports Medicine, Inc.2011—
+1K230517Legends Orthopedics Suture Anchors (Legends Orthopedics 5.5 mm Suture Anchors…Jarmon Medical, LLC (Dba Legends Orthopedics)2023—
+1K192949Flower Suture Anchor SetFlower Orthopedics Corporation2020—
+2K182736OIC Suture Anchor SystemThe Orthopaedic Implant Company2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199520
199610
199830
200150
200210
200420
200620
200720
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201120
201810
202010
202310
FIG. 1 — Lineage of K111590, 1996–2023Source: 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
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
*K110229Rog Suture Anchor 5.5MM, 2.9MMRog Sports Medicine, Inc.2011—
*K110230Rog Knotless Suture AnchorRog Sports Medicine, Inc.2011—

Also cleared against K110229: 1 other device →

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K113299Rog Suture AnchorRog Sports Medicine, Inc.20112
K112991Modified Rog Suture AnchorRog Sports Medicine, Inc.20111
K230517Legends Orthopedics Suture Anchors (Legends Orthopedics 5.5 mm Suture Anchors, Legends…Jarmon Medical, LLC (Dba Legends Orthopedics)20230
K192949Flower Suture Anchor SetFlower Orthopedics Corporation20200

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 4 companies; a new generation was cleared every 2.7 years on median.
  • 7 of the 25 ancestors have a recall of any class.
  • Of its descendants, K113299 (Rog Sports Medicine, Inc., 2011) has gone furthest, with 2 descendants of its own.
  • 1 other device also cites its predicate K110229.

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. 2011, 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 RoG TM 5.5 mm Suture Anchor is indicated for soft tissue reattachment procedures in the shoulder, elbow, wrist/hand, foot/ankle and knee. Specific indications are as follows: * Shoulder indications:- Bankart repair, rotator cuff repair, SLAP lesion repair, capsule repair or capsulolabral reconstruction, acromio-clavicular separation, deltoid repair, biceps tenodesis. * Wrist/hand indications:- Ulnar/Radial collateral ligament reconstruction…

Read the full statement (321 words)

The RoG TM 5.5 mm Suture Anchor is indicated for soft tissue reattachment procedures in the shoulder, elbow, wrist/hand, foot/ankle and knee. Specific indications are as follows:

* Shoulder indications:- Bankart repair, rotator cuff repair, SLAP lesion repair, capsule repair or capsulolabral reconstruction, acromio-clavicular separation, deltoid repair, biceps tenodesis.

* Wrist/hand indications:- Ulnar/Radial collateral ligament reconstruction, scapholunate ligament reconstruction.

* Foot/Ankle indications:- Achilles tendon repair/reconstruction, haliax valgus reconstruction, lateral stabilization, medial stabilization, mid- and forefoot reconstructions.

* Elbow indications:- Biceps tendon reconstruction, ulnar or radial collateral ligament reconstruction, lateral epicondylitis repair.

* Knee indications:- Lateral collateral ligament repair, medial collateral ligament repair, posterior oblique ligament repair, patellar ligament/tendon repair. iliotibial band tenodesis, joint capsule closure.

The RoG 2.9mm Suture Anchor is indicated for use in soft tissue reattachment procedures. Specific indications are as follows:

* Shoulder indications:- Bankart repair, rotator cuff repair, SLAP lesion repair, capsule repair or capsulolabral reconstruction, acromio-clavicular separation, deltoid repair, biceps tenodesis.

* Wrist/hand indications:- Scapholunate ligament reconstruction.

* Elbow indications:- Biceps tendon reconstruction, ulnar or radial collateral ligament reconstruction.

* Knee indications:- Lateral collateral ligament repair, medial collateral ligament repair, posterior oblique ligament repair, patellar ligament/tendon repair. iliotibial band tenodesis, joint capsule closure. extracapsular repair, vastus medialis obliquus (VMO) muscle advancement.

The RoG 5.5 mm Knotless Suture Anchor is indicated for soft tissue reattachment procedures in the shoulder, elbow, wrist/hand, foot/ankle and knee. Specific indications are as follows:

* Shoulder indications:- Bankart repair, rotator cuff repair, SLAP lesion repair, capsule repair or capsulolabral reconstruction, acromio-clavicular separation, deltoid repair, biceps tenodesis.

* Wrist/Hand indications:- Ulnar/Radial collateral ligament reconstruction, scapholunate ligament reconstruction.

* Foot/Ankle indications:- Achilles tendon repair/reconstruction, hallax valgus reconstruction, lateral stabilization, medial stabilization, mid- and forefoot reconstructions.

* Elbow indications:- Biceps tendon reconstruction, ulnar or radial collateral ligament reconstruction, lateral epicondylitis repair.

* Knee indications:- Lateral collateral ligament repair, medial collateral ligament repair, posterior oblique ligament repair, patellar ligament/tendon repair, iliotibial band tenodesis, joint capsule closure.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K111590: Rog Suture Anchor, Rog Knotless Suture Anchor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111590

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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