Vitoss 2102-1105
Vitoss 2102-1105 is an orthopaedic bone void filling material (FDA Class II; FDA product code MQV, Filler, Bone Void, Calcium Compound) made by Stryker Corp., cleared under FDA 510(k) K032288 on 19 Dec 2003 and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 00808232000290), 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 | Number00808232000290 | Date24 Sep 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK032288 | Date19 Dec 2003 | StatusActive |
Official records
- AccessGUDID record 00808232000290
- FDA 510(k) database K032288
Across registries
- FDA 510(k) K032288 decided 19 Dec 2003 Active
- FDA GUDID UDI-DI 00808232000290 listed 24 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K032288
- Listed FDA GUDID 00808232000290
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vitoss
- Generic name
- Orthopaedic bone void filling material, synthetic/animal-derived
- Model / Ref / Catalog
- 2102-1105
- Primary DI / UDI-DI
- 00808232000290
- 510(k) Number
- FDA product code
- MQV
- GMDN term
- Orthopaedic bone void filling material, synthetic/animal-derived
- Device class
- Class II
- Regulation number
- 888.3045
- GUDID distribution status
- In Commercial Distribution
- Size
- Height — 4.0 MillimeterLength — 50.0 MillimeterWidth — 25.0 Millimeter
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