AccuPort End Delivery Cannula 15 Ga x 60 mm Drill Length 308.151

GUDID 00889024205239

ZIMMER KNEE CREATIONS, INC.

Bone grafting cannula
Primary Device ID00889024205239
NIH Device Record Keye44357e3-e17b-4a7f-b252-88681e81eb67
Commercial Distribution StatusIn Commercial Distribution
Brand NameAccuPort End Delivery Cannula 15 Ga x 60 mm Drill Length
Version Model Number308.151
Catalog Number308.151
Company DUNS078836317
Company NameZIMMER KNEE CREATIONS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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

Customer Support Contacts

Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com
Phone484-887-8902
EmailKC.Customerservice@zimmerbiomet.com

Device Dimensions

Needle Gauge15 Gauge

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024205239 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FGYCannula, Injection
FMFSyringe, Piston

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-02-25
Device Publish Date2016-05-19

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