Microfuse Bone Void Filler
510(k) K071187
Microfuse Bone Void Filler is a Class II device made by Globus Medical, Inc., cleared under FDA 510(k) K071187 on 20 Dec 2007, active as of 22 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 | NumberK071187 | Date20 Dec 2007 | StatusActive |
Official records
- FDA 510(k) database K071187
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MQV
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3045
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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