Lumbar Interbody Spacer 300-09

GUDID B114300090

9mm Lumbar PEEK inter-vertebral body spacer

CALVARY SPINE, LLC

Polymeric spinal interbody fusion cage
Primary Device IDB114300090
NIH Device Record Keycd900b20-37dd-4e16-850d-52e687c6f54a
Commercial Distribution StatusIn Commercial Distribution
Brand NameLumbar Interbody Spacer
Version Model Number9mm Straight
Catalog Number300-09
Company DUNS832116532
Company NameCALVARY SPINE, LLC
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone786-301-8006
Emailjames.r.edw@gmail.com
Phone786-301-8006
Emailjames.r.edw@gmail.com

Device Dimensions

Height9 Millimeter
Height9 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB114300090 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B114300090]

Moist Heat or Steam Sterilization


[B114300090]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-02-24
Device Publish Date2016-03-01

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