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Zavation

FDA UDI

Class II (US FDA UDI)

by Zavation

Identity

Trade Name
ZAVATION FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
PLIF 9mmx23mmx0deg -10mm FDA UDI
Model / Reference
570-092300-10 FDA UDI
Description
PLIF 9mmx23mmx0deg -10mm FDA UDI

Identifiers

Primary DI / UDI-DI
00842166167681 FDA UDI
510(k) Number
K211306 FDA UDI
FDA Product Code
MAX FDA UDI
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

No

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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Polymeric spinal interbody fusion cage

Zavation by Zavation — 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
Zavation

Sources (1)

  • FDA UDI 3d56d4ee-1b34-47f6-848b-df6728e1d0f4 35 fields · synced May 30, 2026