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130 Deg Ext Fem Neck Fix Plate, 5-Hole

FDA UDI

Class II (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
130 DEG EXT FEM NECK FIX PLATE, 5-HOLE FDA UDI
Generic Name
Femoral neck fixation plate/sleeve FDA UDI
Device Name
130 DEG EXT FEM NECK FIX PLATE, 5-HOLE FDA UDI
Model / Reference
324-31305 FDA UDI
Description
130 DEG EXT FEM NECK FIX PLATE, 5-HOLE FDA UDI

Identifiers

Catalog Number
324-31305 FDA UDI
Primary DI / UDI-DI
00810189110717 FDA UDI
510(k) Number
K230764 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
Femoral neck fixation plate/sleeve 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 126 Millimeter FDA UDI

Category: Femoral neck fixation plate/sleeve

130 Deg Ext Fem Neck Fix Plate, 5-Hole by OsteoCentric Technologies, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femoral neck fixation plate/sleeve.

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 a056d931-7e3d-44cd-b2ff-2be57742f7dd 37 fields · synced May 30, 2026