MBlock Adjustable Loop BTB
by S.B.M
MBlock Adjustable Loop BTB (05.05.0117) is a Class II device made by S.B.M, cleared under FDA 510(k) K202193 on 16 Oct 2020 and listed in FDA GUDID since 16 Nov 2020 (UDI-DI 03760304680304), 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 | Number03760304680304 | Date16 Nov 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK202193 | Date16 Oct 2020 | StatusActive |
Official records
- AccessGUDID record 03760304680304
- FDA 510(k) database K202193
Across registries
- FDA 510(k) K202193 decided 16 Oct 2020 Active
- FDA GUDID UDI-DI 03760304680304 listed 16 Nov 2020 Listed
Timeline
- Cleared FDA 510(k) K202193
- Listed FDA GUDID 03760304680304
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MBlock
- Generic name
- Tendon/ligament bone anchor, non-bioabsorbable
- Model / Ref / Catalog
- Adjustable Loop BTB, 05.05.0117
- Primary DI / UDI-DI
- 03760304680304
- 510(k) Number
- FDA product code
- MBI
- GMDN term
- Tendon/ligament bone anchor, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
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