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Impulse™ PSI Interbody Fusion System

FDA UDI

Class II (US FDA UDI)

by Degen Medical

Identity

Trade Name
Impulse™ PSI Interbody Fusion System FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
Impulse™ PSI D Shape Spacer FDA UDI
Model / Reference
1704 FDA UDI
Description
Impulse™ PSI D Shape Spacer FDA UDI

Identifiers

Catalog Number
1704 FDA UDI
Primary DI / UDI-DI
00842048181767 FDA UDI
510(k) Number
K241077 FDA UDI
FDA Product Code
MAX 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Metallic spinal interbody fusion cage

Impulse™ PSI Interbody Fusion System by Degen Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Degen Medical

Sources (1)

  • FDA UDI ccae8f75-2e5d-4159-bd06-f124878bb8eb 36 fields · synced May 30, 2026