510(k) · Cleared
ClearedHumerus Locking Plating System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Newclip Technics · HRS Plate, Fixation, Bone
Cleared on Dec 22, 2006 as substantially equivalent to K051728 (Hand Innovations, LLC, 2005) and 3 other predicates after a 73-day review. Its family tree reaches back 3 generations to 2000. 4 later devices descend from it.
- Decided
- Dec 22, 2006
- Review
- 73 days
- Class
- Class II
- Product code
- HRS
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 3 generations to K000684 (2000). 12 ancestors in all, the oldest K890939 (1989). 4 later devices descend from it, 1 citing it directly.
- Root · 3 generations backK000684 Small Fragment Dynamic Compression Locking (DCL) SystemSynthes (Usa) · 2000 · Recalled
- 2 generations backK011335 Synths One-Third Tubular DCL PlateSynthes (Usa) · 2001 · Recalled
- 1 generation backK012655 Congruent Bone Plate SystemAcu Med, Inc. · 2001 · Recalled
- This deviceK063095 Humerus Locking Plating SystemNewclip Technics · 2006
- Descendant · cites it directly · 3 of its ownK141548 High Tibial Osteotomy SystemNewclip Technics · 2015
- Descendant · 2 generations on · 1 of its ownK173746 Activmotion RangeNewclip Technics · 2018
- Descendant · 3 generations on · 0 of its ownK241539 Activmotion SNewclip Technics · 2024
- Descendant · 2 generations on · 0 of its ownK213214 Xpert WristNewclip Technics · 2021
Most influential descendants
Showing 4 of 4 · See all- K141548High Tibial Osteotomy SystemNewclip Technics · 2015 · cites it directly3descendants
- K173746Activmotion RangeNewclip Technics · 2018 · 2 generations on1descendant
- K241539Activmotion SNewclip Technics · 2024 · 3 generations on0descendants
- K213214Xpert WristNewclip Technics · 2021 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K000684 | Small Fragment Dynamic Compression Locking (DCL) System | Synthes (Usa) | 2000 | 1 |
| −2 | K011335 | Synths One-Third Tubular DCL Plate | Synthes (Usa) | 2001 | 2 |
| −1 | K012655 | Congruent Bone Plate System | Acu Med, Inc. | 2001 | 16 |
| 0 (this device) | K063095 | Humerus Locking Plating System | Newclip Technics | 2006 | — |
| +1 | K141548 | High Tibial Osteotomy System | Newclip Technics | 2015 | — |
| +2 | K173746 | Activmotion Range | Newclip Technics | 2018 | — |
| +3 | K241539 | Activmotion S | Newclip Technics | 2024 | — |
| +2 | K213214 | Xpert Wrist | Newclip Technics | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1989 | 1 | 0 |
| 1991 | 1 | 0 |
| 1995 | 1 | 0 |
| 2000 | 1 | 0 |
| 2001 | 1 | 0 |
| 2004 | 2 | 0 |
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2015 | 1 | 0 |
| 2018 | 1 | 0 |
| 2021 | 1 | 0 |
| 2024 | 1 | 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.
Planning a device in HRS? 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 HRS device
- #1 K222465 Tyber Medical Anatomical Plating Systemscore 27.5 · 16 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (4)
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 |
|---|---|---|---|
| * | K051728 | Modification to Shoulder Fixation System | 2005 |
| * | K041860 | Synthes (Usa) LCP Proximal Humerus Plates, LongSummary page 2…rus. K. Predicate device: * Modified Shoulder Fixation System of HAND INNOVATIONS (KO51728) * SYNTHES LCP® Proximal Humerus Plates, long of SYNTHES (K041860) * Proximal Humerus Plate of ACUMED (K012655) * Stryker Plating System of HOWMEDICA OSTEONICS CORP. (K060798)… | 2004 |
| * | K012655 | Congruent Bone Plate SystemSummary page 2…ulder Fixation System of HAND INNOVATIONS (KO51728) * SYNTHES LCP® Proximal Humerus Plates, long of SYNTHES (K041860) * Proximal Humerus Plate of ACUMED (K012655) * Stryker Plating System of HOWMEDICA OSTEONICS CORP. (K060798)… | 2001 |
| * | K060798 | Stryker Plating SystemSummary page 2…P® Proximal Humerus Plates, long of SYNTHES (K041860) * Proximal Humerus Plate of ACUMED (K012655) * Stryker Plating System of HOWMEDICA OSTEONICS CORP. (K060798) Section 4… | 2006 |
What descends from it? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K141548 | High Tibial Osteotomy System | 2015 | 3 |
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 6 years and passes through 3 companies; a new generation was cleared every 1.2 years on median.
- 4 of the 12 ancestors have a recall of any class.
- Of its descendants, K141548 (Newclip Technics, 2015) has gone furthest, with 3 descendants of its own.
- 3 other devices also cite its predicate K051728.
How does its category compare?
All HRS devicesHRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · HRS
54in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HRS
90in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HRS
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HRS
2,306in 2025
MAUDE reports naming product code HRS, 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 | 63 | 2 | 339 |
| 2008 | 35 | 87 | 11 | 311 |
| 2009 | 47 | 85 | 3 | 435 |
| 2010 | 49 | 100 | 16 | 491 |
| 2011 | 43 | 88 | 5 | 773 |
| 2012 | 59 | 106 | 4 | 1,663 |
| 2013 | 56 | 89 | 11 | 2,643 |
| 2014 | 76 | 57 | 0 | 2,413 |
| 2015 | 56 | 97 | 7 | 3,095 |
| 2016 | 44 | 109 | 5 | 2,276 |
| 2017 | 57 | 122 | 3 | 2,220 |
| 2018 | 40 | 116 | 2 | 2,663 |
| 2019 | 46 | 89 | 25 | 3,359 |
| 2020 | 48 | 88 | 1 | 2,790 |
| 2021 | 40 | 87 | 9 | 2,442 |
| 2022 | 47 | 144 | 3 | 1,700 |
| 2023 | 40 | 120 | 1 | 2,049 |
| 2024 | 54 | 96 | 0 | 1,849 |
| 2025 | 54 | 90 | 1 | 2,306 |
| 2026 | 51 | 82 | 3 | — |
What is it indicated for?
The Humerus Locking Plating System is intended for fractures and fracture dislocations, osteotomies, and non-unions of the proximal humerus.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K063095 · printed Nov 6, 2026
Cite this page
510(k) Report. “K063095: Humerus Locking Plating System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K063095
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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