COMET Lumbar Interbody Fusion Cage

GUDID 04710577041455

PEEK Interbody Fusion Cage

BAUI BIOTECH CO. LTD.

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Primary Device ID04710577041455
NIH Device Record Keya4b35174-ecde-4f41-9bb5-abd05cb31eb8
Commercial Distribution StatusIn Commercial Distribution
Brand NameCOMET Lumbar Interbody Fusion Cage
Version Model Number595-08318
Company DUNS656775504
Company NameBAUI BIOTECH CO. LTD.
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104710577041455 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-14
Device Publish Date2020-10-06

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04710577041547PEEK Interbody Fusion Cage

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