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Monterey AL

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Monterey AL FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
Screw FDA UDI
Model / Reference
480115525 FDA UDI
Description
Screw FDA UDI

Identifiers

Catalog Number
480115525 FDA UDI
Primary DI / UDI-DI
07613327422580 FDA UDI
FDA Product Code
MAX FDA UDI
OVD FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

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

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 25.0 Millimeter FDA UDI

Category: Metallic spinal interbody fusion cage

Monterey AL by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI fc843e6d-7e79-4355-a924-b6e86a2b2646 35 fields · synced Jun 6, 2026