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Ac Device

FDA UDI

Class II (US FDA UDI)

by Lockdown Medical Ltd

Identity

Trade Name
AC DEVICE FDA UDI
Generic Name
Ligament graft, synthetic polymer FDA UDI
Device Name
Lockdown 5cm Acromiaclavicular (AC) Device FDA UDI
Model / Reference
LD050 FDA UDI
Description
Lockdown 5cm Acromiaclavicular (AC) Device FDA UDI

Identifiers

Catalog Number
LD050 FDA UDI
Primary DI / UDI-DI
05060433600005 FDA UDI
510(k) Number
K091207 FDA UDI
FDA Product Code
HTN FDA UDI
GMDN Term
Ligament graft, synthetic polymer 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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 5 Centimeter FDA UDI

Category: Ligament graft, synthetic polymer

Ac Device by Lockdown Medical Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ligament graft, synthetic polymer.

Cleared under the same submission

K091207 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lockdown Medical Ltd

Sources (1)

  • FDA UDI 46fd19f8-17b6-4124-a6dd-c8b9757a1d2c 36 fields · synced May 30, 2026