FDA product code · Orthopedic
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction
1 FDA decision since 2002. 1 recall names this code; it is not Class I.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly Download the data (CSV)
Twenty years of NEK at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.
FDA decisions per year · NEK
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NEK
Too few NEK 510(k)s in any year since 2007 to give a median.
Recalls per year · NEK
1in 2018
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NEK
49in 2025
MAUDE reports naming product code NEK, 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 | 5 | — | 0 | 68 |
| 2008 | 5 | — | 0 | 87 |
| 2009 | 3 | — | 0 | 232 |
| 2010 | 4 | — | 0 | 305 |
| 2011 | 4 | — | 0 | 314 |
| 2012 | 6 | — | 0 | 1,957 |
| 2013 | 6 | — | 0 | 3,497 |
| 2014 | 1 | — | 0 | 1,928 |
| 2015 | 4 | — | 0 | 1,734 |
| 2016 | 3 | — | 0 | 1,528 |
| 2017 | 5 | — | 0 | 799 |
| 2018 | 2 | — | 1 | 179 |
| 2019 | 6 | — | 0 | 37 |
| 2020 | 4 | — | 0 | 31 |
| 2021 | 3 | — | 0 | 23 |
| 2022 | 4 | — | 0 | 8 |
| 2023 | 4 | — | 0 | 14 |
| 2024 | 1 | — | 0 | 36 |
| 2025 | 1 | — | 0 | 49 |
| 2026 | 5 | — | 0 | — |
Planning a device in NEK? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report