510(k) · Cleared
ClearedAltapore
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Baxter Healthcare Corporation · MQV Filler, Bone Void, Calcium Compound
Cleared on Jan 9, 2020 as substantially equivalent to K181225 (Baxter Healthcare Corporation, 2018) and 1 other predicate after a 132-day review. Its family tree reaches back 10 generations to 1996. 4 later devices descend from it.
- Decided
- Jan 9, 2020
- Review
- 132 days
- Class
- Class II
- Product code
- MQV
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 10 generations to K960978 (1996). 42 ancestors in all, the oldest K871773 (1987). 4 later devices descend from it, 4 citing it directly.
- Root · 10 generations backK960978 Wright Plaster of Paris Pellets (Subject to Revision)Wrightmedicaltechnologyinc · 1996
- 6 generations between
- 3 generations backK082166 Mastergraft StripMedtronic Sofamor Danek · 2009
- 2 generations backK140375 Mastergraft Putty, Mastergraft StripMedtronic Sofamor Danek USA, Inc. · 2014
- 1 generation backK181225 AltaporeBaxter Healthcare Corporation · 2018
- This deviceK192363 AltaporeBaxter Healthcare Corporation · 2020
- Descendant · cites it directly · 1 of its ownK201464 Altapore MISBaxter Healthcare Corporation · 2020
- Descendant · cites it directly · 1 of its ownK200640 Altapore ShapeBaxter Healthcare Corporation · 2020
- Descendant · cites it directly · 0 of its ownK241564 Actifuse ABX; Actifuse MIS; Actifuse Shape; ALTAPORE; ALTAPORE…Baxter Healthcare Corporation · 2024
- Descendant · cites it directly · 0 of its ownK233259 XerosynXerothera, Inc. · 2024
Show all 10 generations
- Root · 10 generations backK960978 Wright Plaster of Paris Pellets (Subject to Revision)Wrightmedicaltechnologyinc · 1996
- 9 generations backK980817 Pro Osteon Implant 500R Resorbable Bone Graft Substitute Model…Interpore Intl. · 1998
- 8 generations backK000515 Pro Osteon 200R Resorbable Bone Graft Substitute, Models 2RG051…Interpore Cross Intl. · 2000
- 7 generations backK012751 Healos Bone Graft MaterialOrquest, Inc. · 2001
- 6 generations backK043308 Modification to: Healos Bone Graft MaterialDepuy Spine, Inc. · 2005
- 5 generations backK051386 Mastergraft Putty Bone Void FillerMedtronic Vascular · 2005
- 4 generations backK071813 Mastergraft PuttyMedtronic Sofamor Danek · 2007
- 3 generations backK082166 Mastergraft StripMedtronic Sofamor Danek · 2009
- 2 generations backK140375 Mastergraft Putty, Mastergraft StripMedtronic Sofamor Danek USA, Inc. · 2014
- 1 generation backK181225 AltaporeBaxter Healthcare Corporation · 2018
- This deviceK192363 AltaporeBaxter Healthcare Corporation · 2020
Most influential descendants
Showing 4 of 4 · See all- K201464Altapore MISBaxter Healthcare Corporation · 2020 · cites it directly1descendant
- K200640Altapore ShapeBaxter Healthcare Corporation · 2020 · cites it directly1descendant
- K241564Actifuse ABX; Actifuse MIS; Actifuse Shape; ALTAPORE; ALTAPORE SHAPE; ALTAPORE MISBaxter Healthcare Corporation · 2024 · cites it directly0descendants
- K233259XerosynXerothera, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K960978 | Wright Plaster of Paris Pellets (Subject to Revision) | Wrightmedicaltechnologyinc | 1996 | — |
| −9 | K980817 | Pro Osteon Implant 500R Resorbable Bone Graft Substitute Model Numbers 5RG05… | Interpore Intl. | 1998 | — |
| −8 | K000515 | Pro Osteon 200R Resorbable Bone Graft Substitute, Models 2RG051, 2RG101… | Interpore Cross Intl. | 2000 | — |
| −7 | K012751 | Healos Bone Graft Material | Orquest, Inc. | 2001 | — |
| −6 | K043308 | Modification to: Healos Bone Graft Material | Depuy Spine, Inc. | 2005 | — |
| −5 | K051386 | Mastergraft Putty Bone Void Filler | Medtronic Vascular | 2005 | — |
| −4 | K071813 | Mastergraft Putty | Medtronic Sofamor Danek | 2007 | — |
| −3 | K082166 | Mastergraft Strip | Medtronic Sofamor Danek | 2009 | — |
| −2 | K140375 | Mastergraft Putty, Mastergraft Strip | Medtronic Sofamor Danek USA, Inc. | 2014 | — |
| −1 | K181225 | Altapore | Baxter Healthcare Corporation | 2018 | — |
| 0 (this device) | K192363 | Altapore | Baxter Healthcare Corporation | 2020 | — |
| +1 | K201464 | Altapore MIS | Baxter Healthcare Corporation | 2020 | — |
| +1 | K200640 | Altapore Shape | Baxter Healthcare Corporation | 2020 | — |
| +1 | K241564 | Actifuse ABX; Actifuse MIS; Actifuse Shape; ALTAPORE; ALTAPORE SHAPE; ALTAPORE… | Baxter Healthcare Corporation | 2024 | — |
| +1 | K233259 | Xerosyn | Xerothera, Inc. | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1987 | 1 | 0 |
| 1992 | 1 | 0 |
| 1995 | 2 | 0 |
| 1997 | 1 | 0 |
| 1998 | 2 | 0 |
| 1999 | 1 | 0 |
| 2000 | 2 | 0 |
| 2001 | 2 | 0 |
| 2002 | 4 | 0 |
| 2003 | 4 | 0 |
| 2004 | 3 | 0 |
| 2005 | 2 | 0 |
| 2006 | 2 | 0 |
| 2007 | 2 | 0 |
| 2008 | 2 | 0 |
| 2014 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2020 | 2 | 0 |
| 2024 | 2 | 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? (2)
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 |
|---|---|---|---|
| * | K181225 | AltaporeSummary page 5…Table 2. Predicate Devices Device Company Predicate 510(k) Clearance Date ALTAPORE Baxter Healthcare K181225 August 31, 2018 (Predicate Device) Corporation MASTERGRAFT® Medtronic Sofamor K14037… | 2018 |
| * | K140375 | Mastergraft Putty, Mastergraft StripSummary page 5…Baxter Healthcare K181225 August 31, 2018 (Predicate Device) Corporation MASTERGRAFT® Medtronic Sofamor K140375 April 18, 2014 Putty Danek USA, Inc. (Reference Device) The proposed device is substantiall… | 2014 |
What descends from it? (4)
4 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 24 years and passes through 9 companies; a new generation was cleared every 2.0 years on median.
- 6 of the 42 ancestors have a recall of any class.
- Of its descendants, K201464 (Baxter Healthcare Corporation, 2020) has gone furthest, with 1 descendant of its own.
- 1 other device also cites its predicate K181225.
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. 2020, 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?
ALTAPORE is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities, posterolateral spine and pelvis). ALTAPORE can be used by itself, with autograft as a bone graft extender or with autogenous bone marrow aspirate. 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. ALTAPORE resorbs and is replaced with bone during the healing process.
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/K192363 · printed Nov 6, 2026
Cite this page
510(k) Report. “K192363: Altapore.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192363
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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