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Genesys Crossft

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
GENESYS CROSSFT FDA UDI
Generic Name
Tendon/ligament bone anchor, bioabsorbable FDA UDI
Device Name
GENESYS CROSSFT 6.5MM SUTURE ANCHOR, W/ 3 HI-FI #2 (5 METRIC) SUTURES W/NEEDLES FDA UDI
Model / Reference
CFBC-6503N FDA UDI
Description
GENESYS CROSSFT 6.5MM SUTURE ANCHOR, W/ 3 HI-FI #2 (5 METRIC) SUTURES W/NEEDLES FDA UDI

Identifiers

Catalog Number
CFBC-6503N FDA UDI
Primary DI / UDI-DI
10845854034620 FDA UDI
510(k) Number
K101100 FDA UDI
FDA Product Code
MAI FDA UDI
GMDN Term
Tendon/ligament bone anchor, bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Dimensions & Sizes

Size
Outer Diameter — 6.5 Millimeter FDA UDI

Genesys Crossft by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K101100 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 0d2257d4-1755-482f-bc37-9ea41ecbc114 39 fields · synced May 31, 2026