← Back to catalogue

MOJAVE Expandable Interbody System

FDA UDI

Class II (US FDA UDI)

by K2m, Inc.

Identity

Trade Name
MOJAVE Expandable Interbody System FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
Convex Trial, Size 11x24/28x11 mm FDA UDI
Model / Reference
7012-90058 FDA UDI
Description
Convex Trial, Size 11x24/28x11 mm FDA UDI

Identifiers

Catalog Number
7012-90058 FDA UDI
Primary DI / UDI-DI
10888857383982 FDA UDI
FDA Product Code
MQP FDA UDI
ODP FDA UDI
MAX FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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
Height — 11 Millimeter FDA UDI
Length — 28 Millimeter FDA UDI
Width — 11 Millimeter FDA UDI

Category: General internal orthopaedic fixation system implantation kit

MOJAVE Expandable Interbody System by K2m, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
K2m, Inc.

Sources (1)

  • FDA UDI 61be0621-121e-47b8-be5f-439b7fc380e1 36 fields · synced May 31, 2026