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Ibd Peek-C

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
IBD PEEK-C FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
PEEK Cervical Spacer FDA UDI
Model / Reference
48807100 FDA UDI
Description
PEEK Cervical Spacer FDA UDI

Identifiers

Catalog Number
48807100 FDA UDI
Primary DI / UDI-DI
07613327281613 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

Dimensions & Sizes

Size
Width — 16.0 Millimeter FDA UDI
Depth — 14.0 Millimeter FDA UDI
Angle — 0.0 degree FDA UDI
Height — 10.0 Millimeter FDA UDI

Category: Polymeric spinal interbody fusion cage

Ibd Peek-C by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric 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 e8f2b94b-a025-4e93-8bbf-8a5eb2faad10 35 fields · synced May 30, 2026