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3DMetal Diaphyseal Femoral Cones

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
3DMetal Diaphyseal Femoral Cones FDA UDI
Generic Name
Knee arthroplasty wedge FDA UDI
Device Name
3DMetal Diaphyseal Femoral Cone Size Extra Large FDA UDI
Model / Reference
02.07.FCXL30 FDA UDI
Description
3DMetal Diaphyseal Femoral Cone Size Extra Large FDA UDI

Identifiers

Primary DI / UDI-DI
07630971259249 FDA UDI
510(k) Number
K200075 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Knee arthroplasty wedge FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
Commercial Distribution
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

Category: Knee arthroplasty wedge

3DMetal Diaphyseal Femoral Cones by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee arthroplasty wedge.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1b7d04a2-eec4-47e3-82a4-95725382166f 34 fields · synced Jun 6, 2026