Propel 5020210
Propel 5020210 is a Class II device made by NuVasive, LLC, cleared under FDA 510(k) K103036 on 10 Jan 2011 and listed in FDA GUDID since 20 Dec 2018 (UDI-DI 00887517970459), 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 | Number00887517970459 | Date20 Dec 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK103036 | Date10 Jan 2011 | StatusActive |
Official records
- AccessGUDID record 00887517970459
- FDA 510(k) database K103036
Across registries
- FDA 510(k) K103036 decided 10 Jan 2011 Active
- FDA GUDID UDI-DI 00887517970459 listed 20 Dec 2018 Listed
Timeline
- Cleared FDA 510(k) K103036
- Listed FDA GUDID 00887517970459
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Propel
- Generic name
- Human-derived demineralized bone matrix implant
- Model / reference
- 5020210
- Primary DI / UDI-DI
- 00887517970459
- 510(k) Number
- FDA product code
- MBP, MQV
- GMDN term
- Human-derived demineralized bone matrix implant
- Device class
- Class II
- Regulation number
- 888.3045
- GUDID distribution status
- In Commercial Distribution
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- GRAFTON DBM by Osteotech, Inc.