Extentrac
510(k) K980021
Extentrac is a Class II device made by Advanced Back Technologies, cleared under FDA 510(k) K980021 on 11 May 1998, active as of 11 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 | NumberK980021 | Date11 May 1998 | StatusActive |
Official records
- FDA 510(k) database K980021
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JFB
- Device class
- Class II
- Regulation
- 21 CFR Part 890.5880
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
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