ComposiTCP 60 flat head
by S.B.M 4 variants
Ref 905262Model Absorbable interference screw, 60% TCP + 40% PLDLLA, Fully threaded
ComposiTCP 60 flat head (905262) is a device classified as Class III in the EU and Class II in the US made by S.B.M, registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI B-03760154006729), cleared under FDA 510(k) K122228 on 3 Oct 2012 (1 earlier submission) and listed in FDA GUDID since 23 Sep 2015 (UDI-DI 03760154006729), active as of 25 Oct 2026.
Active
CE MDD 510(k)
Valid until
No date given
FDA recalls
None ongoingTrust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-03760154006729 03760154006729 | Date8 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number03760154006729 | Date23 Sep 2015 | StatusListed |
| United States | FDA 510(k)SESE GUDID | NumberK122228 | Date3 Oct 2012 | StatusActive |
Official records
- EUDAMED public site B-03760154006729
- AccessGUDID record 03760154006729
- FDA 510(k) database K122228
- FDA 510(k) database K070507
Across registries
- EUDAMED Basic UDI-DI B-03760154006729 registered 8 Oct 2026 Active
- FDA 510(k) K122228 decided 3 Oct 2012 Active
- FDA GUDID UDI-DI 03760154006729 listed 23 Sep 2015 Listed
Recalls
-
- Completed Z-1361-2022
Mislabeled product.
Timeline
- Cleared FDA 510(k) K070507
- Cleared FDA 510(k) K122228
- Listed FDA GUDID 03760154006729
- Recall initiated FDA recalls Z-1361-2022
- Registered EUDAMED B-03760154006729
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- ComposiTCP
- Generic name
- Bioabsorbable orthopaedic bone screw
- Model / Ref / Catalog
- Absorbable interference screw, 60% TCP + 40% PLDLLA, Fully threaded, 905262, ComposiTCP 60 flat head
- Primary DI / UDI-DI
- 03760154006729
- Basic UDI-DI
- B-03760154006729
- FDA product code
- MAI
- EMDN code
- P09120605 Interference screws
- GMDN term
- Bioabsorbable orthopaedic bone screw
- Device class
- Class III EUDAMEDClass II GUDID
- Regulation number
- 888.3030
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Size
- Length — 35 MillimeterOuter Diameter — 10 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | Absorbable interference screw, 60% TCP + 40% PLDLLA, Fully threaded 905262 | ComposiTCP 60 flat head |
| Device class | Class III | Class II |
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