510(k) · Cleared
ClearedOssipro Bone Substitute Material
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Etex Corp. · MQV Filler, Bone Void, Calcium Compound
Cleared on Jun 28, 2007 as substantially equivalent to K033138 (Etex Corp., 2003) and 1 other predicate after a 296-day review. Its family tree reaches back 2 generations to 2001. 26 later devices descend from it.
- Decided
- Jun 28, 2007
- Review
- 296 days
- Class
- Class II
- Product code
- MQV
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 2 generations to K011048 (2001). 26 later devices descend from it, 4 citing it directly.
- Root · 2 generations backK011048 BSM Bone Substitute MaterialDePuy Orthopaedics, Inc. · 2001
- 1 generation backK033138 CAP3 Bone Substitute MaterialEtex Corp. · 2003
- This deviceK062630 Ossipro Bone Substitute MaterialEtex Corp. · 2007
- Descendant · cites it directly · 21 of its ownK093447 CarrigenEtex Corp. · 2010
- Descendant · 2 generations on · 10 of its ownK101557 Gamma-BSM, Beta-BSM, Equivabone, CarigenEtex Corp. · 2010
- Descendant · 2 generations on · 9 of its ownK103799 Inqu Paste Mix PlusIsto Technologies, Inc. · 2011
- Descendant · 3 generations on · 8 of its ownK130392 Kinex BioactiveGlobus Medical, Inc. · 2013
- Descendant · 3 generations on · 5 of its ownK102528 N-Force Fixation SystemInnovision, Inc. · 2011
Showing 5 of 26 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 26 · See all- K093447CarrigenEtex Corp. · 2010 · cites it directly21descendants
- K101557Gamma-BSM, Beta-BSM, Equivabone, CarigenEtex Corp. · 2010 · 2 generations on10descendants
- K103799Inqu Paste Mix PlusIsto Technologies, Inc. · 2011 · 2 generations on9descendants
- K130392Kinex BioactiveGlobus Medical, Inc. · 2013 · 3 generations on8descendants
- K102528N-Force Fixation SystemInnovision, Inc. · 2011 · 3 generations on5descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K011048 | BSM Bone Substitute Material | DePuy Orthopaedics, Inc. | 2001 | — |
| −1 | K033138 | CAP3 Bone Substitute Material | Etex Corp. | 2003 | — |
| 0 (this device) | K062630 | Ossipro Bone Substitute Material | Etex Corp. | 2007 | — |
| +1 | K093447 | Carrigen | Etex Corp. | 2010 | — |
| +2 | K101557 | Gamma-BSM, Beta-BSM, Equivabone, Carigen | Etex Corp. | 2010 | — |
| +2 | K103799 | Inqu Paste Mix Plus | Isto Technologies, Inc. | 2011 | — |
| +3 | K130392 | Kinex Bioactive | Globus Medical, Inc. | 2013 | — |
| +3 | K102528 | N-Force Fixation System | Innovision, Inc. | 2011 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2010 | 3 | 0 |
| 2011 | 2 | 0 |
| 2013 | 2 | 0 |
| 2014 | 2 | 0 |
| 2015 | 3 | 0 |
| 2016 | 1 | 0 |
| 2017 | 2 | 0 |
| 2018 | 2 | 0 |
| 2019 | 1 | 0 |
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2022 | 1 | 0 |
| 2023 | 2 | 0 |
| 2024 | 2 | 0 |
| 2025 | 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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K033138 | CAP3 Bone Substitute MaterialSummary page 1…lt Bone Void Filler Device PRODUCT CODE: MQV PREDICATE DEVICE(S): CaP 3 Bone Substitute Material, (K033138) a-BSM® Bone Substitute Material (K0l 1048)… | 2003 |
| * | K011048 | BSM Bone Substitute Material | 2001 |
| Kept off the family tree | K011057 | FDA’s K011057 is Intercept Oral Fluid Drug Test Oral Specimen Collection Device, Model 503-XXXX Our reading of the summary gave K011057, FDA’s number for Intercept Oral Fluid Drug Test Oral Specimen Collection… (OraSure Technologies, Inc.). Its FDA name has none of the distinctive words the summary uses for the device it names, “JAX™ Granules Bone Void Filler”. Kept off the family tree. | 2001 |
What descends from it? (26)
See all 264 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 6 years and passes through 2 companies; a new generation was cleared every 3.6 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K093447 (Etex Corp., 2010) has gone furthest, with 21 descendants of its own.
- 5 other devices also cite its predicate K033138.
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. 2007, 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?
OssiPro Bone Substitute Material is an injectable, self setting, macro-porous, osteoconductive, calcium phosphate bone graft substitute material that is intended for use in filling bone voids or defects of the skeletal system (such as the extremities, spine, and the pelvis) that are not intrinsic to the stability of the bony structure. These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. OssiPro is a bone graft substitute that resorbs and is replaced with new bone during the healing process.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K062630 · printed Nov 6, 2026
Cite this page
510(k) Report. “K062630: Ossipro Bone Substitute Material.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K062630
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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