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SynCage

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
SynCage FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
SYNCAGE EVOLUTION SPACER-SMALL 15MM HEIGHT/6DEG-STERILE FDA UDI
Model / Reference
08.825.104S FDA UDI
Description
SYNCAGE EVOLUTION SPACER-SMALL 15MM HEIGHT/6DEG-STERILE FDA UDI

Identifiers

Catalog Number
08825104S FDA UDI
Primary DI / UDI-DI
10705034760124 FDA UDI
510(k) Number
K122639 FDA UDI
FDA Product Code
MAX 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Polymeric spinal interbody fusion cage

SynCage by Synthes — 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
Synthes

Sources (1)

  • FDA UDI f21b5f3b-df99-48e8-a752-9f94d6c1fd88 36 fields · synced May 30, 2026