510(k) · Cleared
Recalled · Class II · 2014VBB System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Synthes · NDN Cement, Bone, Vertebroplasty
Cleared on Dec 13, 2011 as substantially equivalent to K093463 (Care Fusion, 2010) and 6 other predicates after a 285-day review. Its family tree reaches back 5 generations to 2000. 1 later device descends from it. It has been recalled once.
- Decided
- Dec 13, 2011
- Review
- 285 days
- Class
- Class II
- Product code
- NDN
- Recalls
- 1
- Predicates
- 7
Its longest line of descent runs back 5 generations to K001134 (2000). 17 ancestors in all, the oldest K981251 (1998). 1 later device descends from it, 1 citing it directly.
- Root · 5 generations backK001134 Gazelle Balloon Dilatation CatheterBoston Scientific Corp · 2000
- 4 generations backK021735 Boston Scientific Ultra-Soft SV Balloon Dilatation CatheterBoston Scientific Scimed, Inc. · 2002 · Recalled
- 3 generations backK050389 Ultra-Soft SV Balloon Dilatation CatheterBoston Scientific Corp · 2005
- 2 generations backK053116 Sterling Otw Pta Balloon Dilatation Catheter, Model H74939032-XxxxxxBoston Scientific Corp · 2005
- 1 generation backK080982 Sterling ES Monorail and Over-the-Wire Pta Balloon Dilatation…Boston Scientific Corp · 2008
- This deviceK110604 VBB SystemSynthes · 2011
- Descendant · cites it directly · 0 of its ownK130146 Synthes Synflate Vertevral Balloon SystemSynthes (Usa), LLC · 2013
Most influential descendants
Showing 1 of 1 · See all- K130146Synthes Synflate Vertevral Balloon SystemSynthes (Usa), LLC · 2013 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K001134 | Gazelle Balloon Dilatation Catheter | Boston Scientific Corp | 2000 | — |
| −4 | K021735 | Boston Scientific Ultra-Soft SV Balloon Dilatation Catheter | Boston Scientific Scimed, Inc. | 2002 | 23 |
| −3 | K050389 | Ultra-Soft SV Balloon Dilatation Catheter | Boston Scientific Corp | 2005 | — |
| −2 | K053116 | Sterling Otw Pta Balloon Dilatation Catheter, Model H74939032-Xxxxxx | Boston Scientific Corp | 2005 | — |
| −1 | K080982 | Sterling ES Monorail and Over-the-Wire Pta Balloon Dilatation Catheters | Boston Scientific Corp | 2008 | — |
| 0 (this device) | K110604 | VBB System | Synthes | 2011 | — |
| +1 | K130146 | Synthes Synflate Vertevral Balloon System | Synthes (Usa), LLC | 2013 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
| 1999 | 1 | 0 |
| 2000 | 1 | 0 |
| 2001 | 1 | 0 |
| 2003 | 1 | 0 |
| 2004 | 2 | 0 |
| 2005 | 2 | 0 |
| 2009 | 1 | 0 |
| 2010 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 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 NDN? 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 NDN device
- #1 K241775 XeliteMed VertehighFix High Viscosity Spinal…score 14.9 · 4 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (7)
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 |
|---|---|---|---|
| * | K093463 | Avamax Vertebral Balloon Model VBS1010, VBS1015, VBS1020Summary page 1…paedic and Rehabilitation Devices Panel Product Code: NDN, HRX Predicate Devices: CareFusion Avamax (K093463) Kyphon KyphX Xpander Inflatable Bone Tamp (K04 1454)… | 2010 |
| * | K041454 | Kyphx Xpander Inflatable Bone Tamps Model#KO8A,KO9A,K13ASummary page 1…: NDN, HRX Predicate Devices: CareFusion Avamax (K093463) Kyphon KyphX Xpander Inflatable Bone Tamp (K04 1454) Stryker iVAS (K0934 19) Cardinal Health… | 2004 |
| * | K093419 | Ivas 2-10MM (10 Gauge) Balloon Catheter, Ivas 2-15 MM (10 Gauge)0705-115-500, Ivas…Summary page 1…amax (K093463) Kyphon KyphX Xpander Inflatable Bone Tamp (K04 1454) Stryker iVAS (K0934 19) Cardinal Health Inflatablc Bone Tamp (K09021 1)… | 2010 |
| * | K090211 | Inflatable Bone TampSummary page 1…one Tamp (K04 1454) Stryker iVAS (K0934 19) Cardinal Health Inflatablc Bone Tamp (K09021 1) Boston Scientific Sterling Monorail PTA Balloon Dilatation Catheters… | 2009 |
| * | K053118 | Sterling Monorail Pta Balloon Dilatation Catheter, Model H74939031-Xxxxxx | 2005 |
| * | K080982 | Sterling ES Monorail and Over-the-Wire Pta Balloon Dilatation CathetersSummary page 1…) Boston Scientific Sterling Monorail PTA Balloon Dilatation Catheters (K05311I8, K080982) Synthes Click'X (K992739) Device Description: The VBB System… | 2008 |
| * | K992739 | Click'xSummary page 1…ng Monorail PTA Balloon Dilatation Catheters (K05311I8, K080982) Synthes Click'X (K992739) Device Description: The VBB System consists of a Vertebral Body Balloon Catheter,… | 2000 |
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 |
|---|---|---|---|
| K130146 | Synthes Synflate Vertevral Balloon System | 2013 | 0 |
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Oct 6, 2014 | Class II | Z-0877-2015 | Device Design | Additional instructions for use due to inability to raise the pressure above 10 atm during inflation phase may result in an incomplete inflation or delay in procedure |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 11 years and passes through 3 companies; a new generation was cleared every 2.6 years on median.
- 6 of the 17 ancestors have a recall of any class.
- Of its descendants, K130146 (Synthes (Usa), LLC, 2013) has gone furthest, with 0 descendants of its own.
- 3 other devices also cite its predicate K093463.
How does its category compare?
All NDN devicesNDN Cement, Bone, Vertebroplasty: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · NDN
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NDN
90in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NDN
4in 2013
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NDN
626in 2025
MAUDE reports naming product code NDN, 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 | 9 | 128 | 0 | 21 |
| 2008 | 1 | — | 0 | 39 |
| 2009 | 6 | 211 | 1 | 70 |
| 2010 | 5 | 215 | 0 | 396 |
| 2011 | 11 | 164 | 0 | 98 |
| 2012 | 7 | 90 | 0 | 89 |
| 2013 | 7 | 118 | 4 | 242 |
| 2014 | 7 | 106 | 0 | 231 |
| 2015 | 6 | 76 | 0 | 204 |
| 2016 | 4 | 154 | 0 | 182 |
| 2017 | 5 | 125 | 0 | 191 |
| 2018 | 3 | 111 | 0 | 144 |
| 2019 | 2 | — | 0 | 227 |
| 2020 | 4 | 157 | 0 | 212 |
| 2021 | 2 | — | 0 | 344 |
| 2022 | 2 | — | 0 | 270 |
| 2023 | 2 | — | 0 | 311 |
| 2024 | 3 | 90 | 0 | 454 |
| 2025 | 2 | — | 0 | 626 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The Vertebral Body Balloon System is intended to be used for the reduction of fractures and/or creation of a void in cancellous bone in the spine. This includes use during percutaneous vertebral augmentation. The system is to be used with cleared spinal Polymethylmethacrylate (PMMA) bone cements indicated for use during percutaneous vertebral augmentation procedures, such as kyphoplasty.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K110604 · printed Nov 3, 2026
Cite this page
510(k) Report. “K110604: VBB System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K110604
Report an extraction error
Are you the manufacturer?
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