MectaLIF Anterior System

GUDID 07630040708630

Anterior Interbody Fusion Device 24x31x18 L20° - TiPeek

Medacta International SA

Metallic spinal interbody fusion cage
Primary Device ID07630040708630
NIH Device Record Key8cfdf5a1-ecd1-4b14-9ea5-8066d17d8c50
Commercial Distribution StatusIn Commercial Distribution
Brand NameMectaLIF Anterior System
Version Model Number03.31.034
Company DUNS488227125
Company NameMedacta International SA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107630040708630 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-02-24
Device Publish Date2017-04-05

On-Brand Devices [MectaLIF Anterior System]

07630040708630Anterior Interbody Fusion Device 24x31x18 L20° - TiPeek
07630040708623Anterior Interbody Fusion Device 24x31x16 L20° - TiPeek
07630040708616Anterior Interbody Fusion Device 24x31x14 L20° - TiPeek
07630040708609Anterior Interbody Fusion Device 24x31x12 L20° - TiPeek
07630040708524Anterior Interbody Fusion Device 30x40x18 L10° - Peek
07630040708517Anterior Interbody Fusion Device 30x40x16 L10° - Peek
07630040708500Anterior Interbody Fusion Device 30x40x14 L10° - Peek
07630040708494Anterior Interbody Fusion Device 30x40x12 L10° - Peek
07630040708487Anterior Interbody Fusion Device 30x40x10 L10° - Peek
07630040708470Anterior Interbody Fusion Device 30x40x18 L5° - Peek
07630040708463Anterior Interbody Fusion Device 30x40x16 L5° - Peek
07630040708456Anterior Interbody Fusion Device 30x40x14 L5° - Peek
07630040708449Anterior Interbody Fusion Device 30x40x12 L5° - Peek
07630040708432Anterior Interbody Fusion Device 30x40x10 L5° - Peek
07630040708425Anterior Interbody Fusion Device 30x35x18 L20° - Peek
07630040708418Anterior Interbody Fusion Device 30x35x16 L20° - Peek
07630040708401Anterior Interbody Fusion Device 30x35x14 L20° - Peek
07630040708395Anterior Interbody Fusion Device 30x35x18 L15° - Peek
07630040708388Anterior Interbody Fusion Device 30x35x16 L15° - Peek
07630040708371Anterior Interbody Fusion Device 30x35x14 L15° - Peek
07630040708364Anterior Interbody Fusion Device 30x35x12 L15° - Peek
07630040708357Anterior Interbody Fusion Device 30x35x18 L10° - Peek
07630040708340Anterior Interbody Fusion Device 30x35x16 L10° - Peek
07630040708333Anterior Interbody Fusion Device 30x35x14 L10° - Peek
07630040708326Anterior Interbody Fusion Device 30x35x12 L10° - Peek
07630040708319Anterior Interbody Fusion Device 30x35x10 L10° - Peek
07630040708302Anterior Interbody Fusion Device 30x35x18 L5° - Peek
07630040708296Anterior Interbody Fusion Device 30x35x16 L5° - Peek
07630040708289Anterior Interbody Fusion Device 30x35x14 L5° - Peek
07630040708272Anterior Interbody Fusion Device 30x35x12 L5° - Peek
07630040708265Anterior Interbody Fusion Device 30x35x10 L5° - Peek
07630040708258Anterior Interbody Fusion Device 27x35x18 L20° - Peek
07630040708241Anterior Interbody Fusion Device 27x35x16 L20° - Peek
07630040708234Anterior Interbody Fusion Device 27x35x14 L20° - Peek
07630040708227Anterior Interbody Fusion Device 24x31x18 L20° - Peek
07630040708210Anterior Interbody Fusion Device 24x31x16 L20° - Peek
07630040708203Anterior Interbody Fusion Device 24x31x14 L20° - Peek
07630040708197Anterior Interbody Fusion Device 24x31x12 L20° - Peek
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.