Mastergraft Resorbable Ceramic
by Medtronic Sofamor Danek, Inc.
510(k) K020986
Mastergraft Resorbable Ceramic is a Class II device made by Medtronic Sofamor Danek, Inc., cleared under FDA 510(k) K020986 on 22 Jul 2002, 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 | NumberK020986 | Date22 Jul 2002 | StatusActive |
Official records
- FDA 510(k) database K020986
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- Withdrawn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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