icotec Lumbar Cage PLIF 8° / 25 mm x 11 mm 13-59-82511

GUDID 07640164848419

icotec Lumbar Cage PLIF 8° / 25 mm x 11 mm

icotec AG

Polymeric spinal fusion cage, sterile
Primary Device ID07640164848419
NIH Device Record Keyd57ddf79-5835-474a-8ad2-8d441ea66ffc
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Lumbar Cage PLIF 8° / 25 mm x 11 mm
Version Model Number13-59-82511
Catalog Number13-59-82511
Company DUNS480789465
Company Nameicotec AG
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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

Customer Support Contacts

Phone+41717570000
Emailinfo@icotec.ch

Device Identifiers

Device Issuing AgencyDevice ID
GS107640164848419 [Primary]

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 Date2018-08-16
Device Publish Date2018-07-16

On-Brand Devices [icotec Lumbar Cage PLIF 8° / 25 mm x 11 mm]

07640164848419icotec Lumbar Cage PLIF 8° / 25 mm x 11 mm
07640140438276icotec Lumbar Cage PLIF 8° / 25 mm x 11 mm

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