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SYNFIX Evolution

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
SYNFIX Evolution FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
SYNFIX® EVOLUTION SCREW/30MM STERILE FDA UDI
Model / Reference
04.835.230.02S FDA UDI
Description
SYNFIX® EVOLUTION SCREW/30MM STERILE FDA UDI

Identifiers

Catalog Number
0483523002S FDA UDI
Primary DI / UDI-DI
20705034816163 FDA UDI
510(k) Number
K150673 FDA UDI
FDA Product Code
OVD FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable 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

Category: Spinal bone screw, non-bioabsorbable

SYNFIX Evolution by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

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 6fd1b191-9534-42c2-8c11-a0dd0b7b9393 36 fields · synced May 30, 2026