510(k) · Cleared
ClearedNuVasive AttraX Scaffold
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Nu Vasive, Incorporated · MQV Filler, Bone Void, Calcium Compound
Cleared on Nov 24, 2017 as substantially equivalent to K050789 (R and D Medical, LLC, 2005) and 2 other predicates after a 98-day review. Its family tree reaches back 7 generations to 1996. 1 later device descends from it.
- Decided
- Nov 24, 2017
- Review
- 98 days
- Class
- Class II
- Product code
- MQV
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 7 generations to K960978 (1996). 20 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 7 generations backK960978 Wright Plaster of Paris Pellets (Subject to Revision)Wrightmedicaltechnologyinc · 1996
- 6 generations backK980817 Pro Osteon Implant 500R Resorbable Bone Graft Substitute Model…Interpore Intl. · 1998
- 5 generations backK030131 Ossatura BCP Bone Void FillerIsotis NV · 2003
- 4 generations backK040082 Pore-SI Bone Graft SubstituteApatech, Ltd. · 2004
- 3 generations backK071206 Actifuse Abx E-Z-Fil Putty Bone Graft SubstituteApatech, Ltd. · 2007 · Recalled
- 2 generations backK080736 Actifuse Shape Bone Graft SubstituteApatech, Ltd. · 2008
- 1 generation backK151584 AttraX PuttyProgentix Orthobiology BV · 2015
- This deviceK172497 NuVasive AttraX ScaffoldNu Vasive, Incorporated · 2017
- Descendant · cites it directly · 0 of its ownK240507 NuVasive AttraX ScaffoldNuvasive, Inc. · 2024
Most influential descendants
Showing 1 of 1 · See all- K240507NuVasive AttraX ScaffoldNuvasive, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K960978 | Wright Plaster of Paris Pellets (Subject to Revision) | Wrightmedicaltechnologyinc | 1996 | — |
| −6 | K980817 | Pro Osteon Implant 500R Resorbable Bone Graft Substitute Model Numbers 5RG05… | Interpore Intl. | 1998 | — |
| −5 | K030131 | Ossatura BCP Bone Void Filler | Isotis NV | 2003 | — |
| −4 | K040082 | Pore-SI Bone Graft Substitute | Apatech, Ltd. | 2004 | — |
| −3 | K071206 | Actifuse Abx E-Z-Fil Putty Bone Graft Substitute | Apatech, Ltd. | 2007 | 1 |
| −2 | K080736 | Actifuse Shape Bone Graft Substitute | Apatech, Ltd. | 2008 | — |
| −1 | K151584 | AttraX Putty | Progentix Orthobiology BV | 2015 | — |
| 0 (this device) | K172497 | NuVasive AttraX Scaffold | Nu Vasive, Incorporated | 2017 | — |
| +1 | K240507 | NuVasive AttraX Scaffold | Nuvasive, Inc. | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
| 1999 | 1 | 0 |
| 2000 | 2 | 0 |
| 2001 | 3 | 0 |
| 2002 | 1 | 0 |
| 2003 | 2 | 0 |
| 2005 | 1 | 0 |
| 2009 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 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 MQV? 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 MQV device
- #1 K232315 Catalyst Bone Void Fillerscore 25.2 · 25 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K050789 | Formagraft Collagen Bone Graft MatrixSummary page 4…e Devices The subject NuVasive AttraX Scaffold substantially equivalent to the primary predicate device, NuVasive Formagraft™ Collagen Bone Graft Matrix (K050789), and additional predicates NuVasive AttraX Putty (K151584) and NuVasive AttraX Granules 1 (K090641). D. Device Des… | 2005 |
| * | K151584 | AttraX PuttySummary page 4…y equivalent to the primary predicate device, NuVasive Formagraft™ Collagen Bone Graft Matrix (K050789), and additional predicates NuVasive AttraX Putty (K151584) and NuVasive AttraX Granules 1 (K090641). D. Device Description The subject AttraX Scaffold, is an osteoconductive… | 2015 |
| * | K090641 | CuriosSummary page 4…device, NuVasive Formagraft™ Collagen Bone Graft Matrix (K050789), and additional predicates NuVasive AttraX Putty (K151584) and NuVasive AttraX Granules 1 (K090641). D. Device Description The subject AttraX Scaffold, is an osteoconductive and resorbable bone void filler designed… | 2009 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K240507 | NuVasive AttraX Scaffold | 2024 | 0 |
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 21 years and passes through 6 companies; a new generation was cleared every 2.3 years on median.
- 2 of the 20 ancestors have a recall of any class.
- Of its descendants, K240507 (Nuvasive, Inc., 2024) has gone furthest, with 0 descendants of its own.
- 2 other devices also cite its predicate K050789.
How does its category compare?
All MQV devicesMQV Filler, Bone Void, Calcium Compound: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.
FDA decisions per year · MQV
14in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MQV
57in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MQV
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MQV
57in 2025
MAUDE reports naming product code MQV, 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 | 144 | 5 | 67 |
| 2008 | 32 | 102 | 3 | 71 |
| 2009 | 23 | 180 | 1 | 81 |
| 2010 | 17 | 147 | 0 | 68 |
| 2011 | 16 | 92 | 6 | 114 |
| 2012 | 9 | 107 | 3 | 149 |
| 2013 | 12 | 197 | 2 | 223 |
| 2014 | 20 | 153 | 0 | 111 |
| 2015 | 18 | 184 | 0 | 125 |
| 2016 | 8 | 214 | 1 | 106 |
| 2017 | 17 | 124 | 1 | 107 |
| 2018 | 23 | 124 | 2 | 86 |
| 2019 | 13 | 90 | 0 | 65 |
| 2020 | 15 | 132 | 1 | 126 |
| 2021 | 8 | 88 | 0 | 101 |
| 2022 | 9 | 118 | 0 | 47 |
| 2023 | 21 | 74 | 3 | 120 |
| 2024 | 28 | 55 | 2 | 68 |
| 2025 | 14 | 57 | 1 | 57 |
| 2026 | 5 | 96 | 4 | — |
What is it indicated for?
AttraX Scaffold is an implant intended to fill bony voids or gaps of the skeletal system (i.e., posterolateral spine and pelvis). AttraX Scaffold must be used in combination with either autogenous bone or autogenous bone marrow aspirate in the posterolateral spine. These osseous defects may be surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. AttraX Scaffold resorbs and is replaced with bone during the healing process.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K172497 · printed Nov 6, 2026
Cite this page
510(k) Report. “K172497: NuVasive AttraX Scaffold.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K172497
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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