MagnetOs 703-013-US
MagnetOs 703-013-US is an orthopaedic bone void filling material (FDA Class II; FDA product code MQV, Filler, Bone Void, Calcium Compound) made by Kuros Biosciences B.V, cleared under FDA 510(k) K161859 on 24 Feb 2017 and listed in FDA GUDID since 8 Jan 2018 (UDI-DI 08719699710122), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08719699710122 | Date8 Jan 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK161859 | Date24 Feb 2017 | StatusActive |
Official records
- AccessGUDID record 08719699710122
- FDA 510(k) database K161859
Across registries
- FDA 510(k) K161859 decided 24 Feb 2017 Active
- FDA GUDID UDI-DI 08719699710122 listed 8 Jan 2018 Listed
Timeline
- Cleared FDA 510(k) K161859
- Listed FDA GUDID 08719699710122
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MagnetOs
- Generic name
- Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
- Model / reference
- 703-013-US
- Primary DI / UDI-DI
- 08719699710122
- 510(k) Number
- FDA product code
- MQV
- GMDN term
- Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
- Device class
- Class II
- Regulation number
- 888.3045
- GUDID distribution status
- In Commercial Distribution
- Size
- Total Volume — 0.5 Centiliter
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- OSTEOSPAN MORPHEUS by Biogennix, LLC
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