← Back to catalogue

MectaLIF

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
MectaLIF FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
MectaLIF Posterior PEEK 9x22x11 L12° FDA UDI
Model / Reference
03.21.238 FDA UDI
Description
MectaLIF Posterior PEEK 9x22x11 L12° FDA UDI

Identifiers

Primary DI / UDI-DI
07630345728326 FDA UDI
510(k) Number
K212831 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Metallic 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

Category: Metallic spinal interbody fusion cage

MectaLIF by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1216d084-460b-493b-a6cb-8551d2994a28 34 fields · synced Jun 8, 2026