SLiK Anchor 10918
SLiK Anchor 10918 is a Class II device made by Parcus Medical LLC, cleared under FDA 510(k) K170327 on 30 Mar 2017 and listed in FDA GUDID since 29 Nov 2017 (UDI-DI M685109181), 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 | NumberM685109181 | Date29 Nov 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK170327 | Date30 Mar 2017 | StatusActive |
Official records
- FDA 510(k) database K170327
Across registries
- FDA 510(k) K170327 decided 30 Mar 2017 Active
- FDA GUDID UDI-DI M685109181 listed 29 Nov 2017 Listed
Timeline
- Cleared FDA 510(k) K170327
- Listed FDA GUDID M685109181
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- SLiK Anchor
- Generic name
- Tendon/ligament bone anchor, non-bioabsorbable
- Model / Ref / Catalog
- 10918
- Primary DI / UDI-DI
- M685109181
- 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
- MRI safety
- MR Safe
- Size
- Length — 15 MillimeterOuter Diameter — 5.5 Millimeter
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