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Ligament Staple

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
Ligament Staple FDA UDI
Generic Name
Orthopaedic bone staple, non-adjustable FDA UDI
Device Name
k-wire KIT for Ligament Staple L105mm FDA UDI
Model / Reference
05.12.10.0006 FDA UDI
Description
k-wire KIT for Ligament Staple L105mm FDA UDI

Identifiers

Primary DI / UDI-DI
07630345719133 FDA UDI
510(k) Number
K210456 FDA UDI
FDA Product Code
JDR FDA UDI
GMDN Term
Orthopaedic bone staple, non-adjustable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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: Orthopaedic bone staple, non-adjustable

Ligament Staple by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone staple, non-adjustable.

Cleared under the same submission

K210456 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e6a7bdac-223f-4477-bff2-b9bb17d3b174 34 fields · synced May 30, 2026