510(k) Report

510(k) · Cleared

Cleared

JAWS Nitinol Staple System

K230550510(k) TraditionalCleared May 11, 202372-day reviewClass II21 CFR 888.3030

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

Paragon 28, Inc. · JDR Staple, Fixation, Bone

Cleared on May 11, 2023 as substantially equivalent to K223056 (Paragon 28, Inc., 2023) after a 72-day review. Its family tree reaches back 3 generations to 2001. 1 later device descends from it.

Decided
May 11, 2023
Review
72 days
Class
Class II
Product code
JDR
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K001354 (2001). 6 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2013: 1 other ancestor2006: 1 other ancestor2001: 1 other ancestor2026: 1 descendant clearedK001354 · Memograph; Osstaple - Orthopedic Uses for Small Bone and Fragment Fixation for the Memograph Staple System · Biomedical Ent., Inc. · 2001K170923 · JAWS (TM) Nitinol Staple System · Paragon 28 · 2017 · recalledK223056 · JAWS Nitinol Staple System · Paragon 28, Inc. · 2023200020052010201520202025
  1. Root · 3 generations backK001354 Memograph; Osstaple - Orthopedic Uses for Small Bone and Fragment…Biomedical Ent., Inc. · 2001
  2. 2 generations backK170923 JAWS (TM) Nitinol Staple SystemParagon 28 · 2017 · Recalled
  3. 1 generation backK223056 JAWS Nitinol Staple SystemParagon 28, Inc. · 2023
  4. This deviceK230550 JAWS Nitinol Staple SystemParagon 28, Inc. · 2023
  5. Descendant · cites it directly · 0 of its ownK261121 Megalodon Dynamic Compression SystemParagon 28, Inc. · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K261121Megalodon Dynamic Compression SystemParagon 28, Inc. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K001354Memograph; Osstaple - Orthopedic Uses for Small Bone and Fragment Fixation for…Biomedical Ent., Inc.2001—
−2K170923JAWS (TM) Nitinol Staple SystemParagon 2820171
−1K223056JAWS Nitinol Staple SystemParagon 28, Inc.2023—
0 (this device)K230550JAWS Nitinol Staple SystemParagon 28, Inc.2023—
+1K261121Megalodon Dynamic Compression SystemParagon 28, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110
200610
201310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K230550, 2001–2026Source: 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 JDR? 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 JDR device

  1. #1 K243658 TMC Compression Implant Systemscore 16.7 · 18 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
*K223056JAWS Nitinol Staple System
Summary page 4
…modate a variety of small bone applications. The implants and instruments are sold sterile. Predicate Device: JAWS® Nitinol Staple System (K223056) Paragon 28, Inc. 1…
Paragon 28, Inc.2023—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K261121Megalodon Dynamic Compression SystemParagon 28, Inc.20260

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 22 years and passes through 3 companies; a new generation was cleared every 5.6 years on median.
  • 1 of the 6 ancestors has a recall of any class.
  • Of its descendants, K261121 (Paragon 28, Inc., 2026) has gone furthest, with 0 descendants of its own.

How does its category compare?

All JDR devices

JDR Staple, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · JDR

3in 2025

2007: 82008: 52010: 22011: 12012: 12013: 92014: 112015: 72016: 62017: 92018: 82019: 52020: 42021: 32022: 52023: 92024: 42025: 32026 (partial year): 2
2007high 11 (2014) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JDR

65in 2025

2007: 70 days median2008: 89 days median2013: 137 days median2014: 97 days median2015: 111 days median2016: 101 days median2017: 172 days median2018: 107 days median2019: 149 days median2020: 161 days median2021: 62 days median2022: 107 days median2023: 72 days median2024: 29 days median2025: 65 days median
2007high 172 (2017) · low 29 (2024)2026

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

Recalls per year · JDR

11in 2022

2008: 12015: 12018: 12020: 12022: 112026 (partial year): 2
2007high 11 (2022) · low 0 (2007)2026

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

Adverse event reports per year · JDR

314in 2025

2007: 32008: 142009: 102010: 352011: 622012: 342013: 272014: 492015: 482016: 762017: 1162018: 2392019: 2422020: 2342021: 2102022: 2022023: 1752024: 2062025: 314
2007high 314 (2025) · low 3 (2007)2025

MAUDE reports naming product code JDR, 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
200787003
2008589114
20090—010
20102—035
20111—062
20121—034
20139137027
20141197049
20157111148
20166101076
201791720116
201881071239
201951490242
202041611234
20213620210
2022510711202
20239720175
20244290206
20253650314
20262—2—

What is it indicated for?

The JAWS® Nitinol Staple System implants are indicated for use in osteotomy, arthrodesis, and fragment fixation of the bones and joints of the foot including fixation of small bone fragments (i.e. small fragments of bone which are not comminuted to the extent to preclude staple placement) located in the long bones of the lower extremities such as the fibula and tibia.

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. “K230550: JAWS Nitinol Staple System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K230550

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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