Identity
- Trade Name
- CUFFLINK Y-KNOT CROSSFT FDA UDI
- Generic Name
- General surgical procedure kit, non-medicated, single-use FDA UDI
- Device Name
- CUFFLINK IMPLANT SYSTEM WITH Y-KNOT RC TAPE AND 5.5MM CROSSFT KNOTLESS FDA UDI
- Model / Reference
- CFK-YT55K FDA UDI
- Description
- CUFFLINK IMPLANT SYSTEM WITH Y-KNOT RC TAPE AND 5.5MM CROSSFT KNOTLESS FDA UDI
Identifiers
- Catalog Number
- CFK-YT55K FDA UDI
- Primary DI / UDI-DI
- 10845854045213 FDA UDI
- 510(k) Number
- K171725 FDA UDI
- FDA Product Code
- MBI FDA UDI
- GMDN Term
- General surgical procedure kit, non-medicated, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Cufflink Y-Knot Crossft by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K171725 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI 7db716b4-8a62-4565-b437-2306f014a836 39 fields · synced May 30, 2026