MagnetOs 703-050-US
MagnetOs 703-050-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) K241212 on 27 Jun 2024 (2 earlier submissions) and listed in FDA GUDID since 29 Sep 2022 (UDI-DI 08719699712102), 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 | FDA 510(k)SESE | NumberK241212 | Date27 Jun 2024 | StatusActive |
| United States | GUDID listing | Number08719699712102 | Date29 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 08719699712102
- FDA 510(k) database K241212
- FDA 510(k) database K233607
- FDA 510(k) database K211201
Across registries
- FDA 510(k) K241212 decided 27 Jun 2024 Active
- FDA GUDID UDI-DI 08719699712102 listed 29 Sep 2022 Listed
Timeline
- Cleared FDA 510(k) K211201
- Listed FDA GUDID 08719699712102
- Cleared FDA 510(k) K233607
- Cleared FDA 510(k) K241212
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- Withdrawn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
- 703-050-US
- Primary DI / UDI-DI
- 08719699712102
- 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
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- APATIGHT-TCP BONE GRAFT SUBSTITUTE by Cerabio, LLC
- HEALOS BONE GRAFT MATERIAL by Orquest, Inc.
- BIOACTIVE BONE GRAFT PUTTY by Biostructures