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Ligafix

FDA UDI

Class II (US FDA UDI)

by S.b.m

Identity

Trade Name
LIGAFIX FDA UDI
Generic Name
Bioabsorbable orthopaedic bone screw FDA UDI
Device Name
Absorbable interference screw FDA UDI
Model / Reference
LIGAFIX 60 round head FDA UDI
Description
Absorbable interference screw FDA UDI

Identifiers

Catalog Number
COM6010030 FDA UDI
Primary DI / UDI-DI
03760154003872 FDA UDI
510(k) Number
K122228 FDA UDI
FDA Product Code
MAI FDA UDI
GMDN Term
Bioabsorbable orthopaedic bone screw 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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 10 Millimeter FDA UDI
Length — 30 Millimeter FDA UDI

Category: Bioabsorbable orthopaedic bone screw

Ligafix by S.b.m — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bioabsorbable orthopaedic bone screw.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
S.b.m

Sources (1)

  • FDA UDI 8009f0c4-c617-4e02-82f3-b6bcc174039a 37 fields · synced Jun 8, 2026