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Integrate-C

FDA UDI

Class II (US FDA UDI)

by Happe Spine

Identity

Trade Name
INTEGRATE-C FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
HAPPE Spine - ACDF INTEGRATE-C Large, 20 x 15 x 8 mm ,7 deg FDA UDI
Model / Reference
Large, 20 x 15 x 8 mm ,7 deg FDA UDI
Description
HAPPE Spine - ACDF INTEGRATE-C Large, 20 x 15 x 8 mm ,7 deg FDA UDI

Identifiers

Catalog Number
08L07 FDA UDI
Primary DI / UDI-DI
G2308H2AF08L070 FDA UDI
510(k) Number
K222004 FDA UDI
FDA Product Code
ODP FDA UDI
GMDN Term
Polymeric 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Polymeric spinal interbody fusion cage

Integrate-C by Happe Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric 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
Happe Spine

Sources (1)

  • FDA UDI ceb5fc3d-bc87-47cb-a99b-2446a1b9c357 36 fields · synced Jun 8, 2026