SpaceOAR Vue System (SV-2101)
FDA 510(k) clearance K260119 · decided 2026-02-10
Clearance details
- K-number
- K260119
- Device name
- SpaceOAR Vue System (SV-2101)
- Applicant
- Boston Scientific Corporation
- Decision
- Substantially Equivalent
- Date received
- 2026-01-14
- Decision date
- 2026-02-10
- Days to decision
- 27 days
- Clearance type
- Special
- Product code
- OVB
- Device class
- 2
- Regulation number
- 892.5725
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Marborough, MA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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| Record | Firm | Date |
|---|---|---|
| BioProtect Balloon Implant™ System (K222972) | Bioprotect, Ltd. | 2023-08-25 |
| Barrigel Injectable Gel (K220641) | Palette Life Sciences | 2022-05-26 |
| SpaceOAR System (K202224) | Boston Scientific Corporation | 2020-08-28 |
| SpaceOAR Vue Hydrogel (K182971) | Augmenix, Inc. | 2019-07-19 |
| SpaceOAR System (K181465) | Augmenix, Inc. | 2018-06-25 |
| SpaceOAR System (DEN140030) | Augmenix, Inc. | 2015-04-01 |
Recalls involving this device
No recalls on record reference this clearance.
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