510(k) · Cleared
ClearedSynthes 7.0/7.3 MM Cannulated Screws
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Synthes (Usa) · HWC Screw, Fixation, Bone
Cleared on Aug 5, 1996 after a 74-day review. The FDA summary names its predicate without a number. 1 of the 739 devices in its family, counting itself, has a Class I recall. 738 later devices descend from it.
- Decided
- Aug 5, 1996
- Review
- 74 days
- Class
- Class II
- Product code
- HWC
- Recalls
- None
- Predicates
- 0
738 later devices descend from it, 27 citing it directly. 1 of the 739 devices in this family, counting this one, has a Class I recall.
- This deviceK962011 Synthes 7.0/7.3 MM Cannulated ScrewsSynthes (Usa) · 1996
- Descendant · cites it directly · 309 of its ownK102903 Pioneer Cannulated Screw SystemPioneer Surgical Technology, Inc. · 2010
- Descendant · cites it directly · 238 of its ownK112028 SI-Lok Sacroiliac Joint Fixation SystemGlobus Medical, Inc. · 2011
- Descendant · cites it directly · 220 of its ownK102343 Emerge Medical Cannulated Screw Fixation SystemEmerge Medical · 2010
- Descendant · 2 generations on · 219 of its ownK103705 Low Profile ScrewsArthrex, Inc. · 2011
- Descendant · cites it directly · 181 of its ownK021233 Aap Cannulated ScrewsAap Implantate AG · 2002
Showing 5 of 738 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K211616 ExcelsiusHub3 generations on · 2021
Most influential descendants
Showing 5 of 738 · See all- K102903Pioneer Cannulated Screw SystemPioneer Surgical Technology, Inc. · 2010 · cites it directly309descendants
- K112028SI-Lok Sacroiliac Joint Fixation SystemGlobus Medical, Inc. · 2011 · cites it directly238descendants
- K102343Emerge Medical Cannulated Screw Fixation SystemEmerge Medical · 2010 · cites it directly220descendants
- K103705Low Profile ScrewsArthrex, Inc. · 2011 · 2 generations on219descendants
- K021233Aap Cannulated ScrewsAap Implantate AG · 2002 · cites it directly181descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K962011 | Synthes 7.0/7.3 MM Cannulated Screws | Synthes (Usa) | 1996 | — |
| +1 | K102903 | Pioneer Cannulated Screw System | Pioneer Surgical Technology, Inc. | 2010 | — |
| +1 | K112028 | SI-Lok Sacroiliac Joint Fixation System | Globus Medical, Inc. | 2011 | — |
| +1 | K102343 | Emerge Medical Cannulated Screw Fixation System | Emerge Medical | 2010 | — |
| +2 | K103705 | Low Profile Screws | Arthrex, Inc. | 2011 | — |
| +1 | K021233 | Aap Cannulated Screws | Aap Implantate AG | 2002 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
| 2002 | 1 | 0 |
| 2007 | 1 | 0 |
| 2008 | 2 | 0 |
| 2009 | 1 | 0 |
| 2010 | 6 | 0 |
| 2011 | 9 | 0 |
| 2012 | 7 | 0 |
| 2013 | 15 | 0 |
| 2014 | 20 | 0 |
| 2015 | 30 | 0 |
| 2016 | 20 | 0 |
| 2017 | 44 | 0 |
| 2018 | 21 | 0 |
| 2019 | 36 | 0 |
| 2020 | 51 | 0 |
| 2021 | 56 | 1 |
| 2022 | 74 | 0 |
| 2023 | 88 | 0 |
| 2024 | 85 | 0 |
| 2025 | 81 | 0 |
| 2026 | 89 | 0 |
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.
1 device in this family has a Class I recall. 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 HWC device
- #1 K203011 Monster Screw Systemscore 22.2 · 14 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | — | Synthes 6.5 mm Cancellous Screws Named without a submission number |
What descends from it? (738)
See all 73827 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K102903 | Pioneer Cannulated Screw System | 2010 | 309 |
| K112028 | SI-Lok Sacroiliac Joint Fixation System | 2011 | 238 |
| K102343 | Emerge Medical Cannulated Screw Fixation System | 2010 | 220 |
| K021233 | Aap Cannulated Screws | 2002 | 181 |
| K082874 | Biodrive Cannulated Screw System | 2009 | 168 |
| K124027 | Monster Screw System | 2013 | 41 |
| K123890 | Acumed Cannulated Screw System | 2013 | 36 |
| K171595 | M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System | 2017 | 35 |
| K161616 | DePuy Synthes 4.0 mm and 4.5 mm Cortex Screws, DePuy Synthes 2.4 mm Cannulated Screws… | 2017 | 33 |
| K131920 | Stabilization Screw | 2014 | 18 |
Has anything in its family been recalled? (1 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K211616ExcelsiusHubGlobus Medical, Inc. · 2021 · 3 generations on · ◆ in the 2021 descendants bar of FIG. 11 Class I recall
What does this lineage say?
- Of its descendants, K102903 (Pioneer Surgical Technology, Inc., 2010) has gone furthest, with 309 descendants of its own.
How does its category compare?
All HWC devicesHWC Screw, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · HWC
15in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HWC
111in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HWC
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HWC
2,893in 2025
MAUDE reports naming product code HWC, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 35 | 77 | 25 | 669 |
| 2008 | 33 | 76 | 33 | 660 |
| 2009 | 27 | 113 | 29 | 651 |
| 2010 | 23 | 110 | 7 | 765 |
| 2011 | 35 | 88 | 12 | 1,104 |
| 2012 | 20 | 99 | 30 | 3,339 |
| 2013 | 25 | 90 | 14 | 3,850 |
| 2014 | 31 | 88 | 2 | 2,549 |
| 2015 | 41 | 85 | 5 | 2,711 |
| 2016 | 26 | 131 | 4 | 2,285 |
| 2017 | 40 | 127 | 4 | 2,561 |
| 2018 | 20 | 106 | 1 | 3,662 |
| 2019 | 30 | 108 | 5 | 5,463 |
| 2020 | 28 | 75 | 4 | 4,820 |
| 2021 | 26 | 84 | 2 | 4,446 |
| 2022 | 26 | 167 | 13 | 3,934 |
| 2023 | 24 | 104 | 0 | 3,718 |
| 2024 | 17 | 90 | 0 | 3,575 |
| 2025 | 15 | 111 | 1 | 2,893 |
| 2026 | 21 | 125 | 2 | — |
What is it indicated for?
Synthes 7.0/7.3 mm Cannulated Screws are generally intended for fracture fixation of large bones and large bone fragments.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K962011 · printed Nov 6, 2026
Cite this page
510(k) Report. “K962011: Synthes 7.0/7.3 MM Cannulated Screws.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K962011
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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