FDA.reportPublic FDA data

Atrix-C Cervical Allograft Spacer

Primary DI
M697X09400050
Brand
Atrix-C Cervical Allograft Spacer
Company
Xtant Medical Holdings, Inc.
Model
X094-0005
Device description
Sterilization Case Atrix-C Instruments
Published
2016-03-29
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
LRPTRAY, SURGICAL

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LRPTray, SurgicalGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
M697X09400050Direct MarkingHIBCC0
M697X09400051PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Cadaveric-donor bone allograftBone intended for transplantation that is harvested from a cadaveric human donor genetically different from the human recipient, typically cadaver bone from a bone bank where donor bone is typically disinfected and stored after stabilization by rapid freezing and dehydration under vacuum conditions (i.e., lyophilization). The bone is permanently implanted during plastic (reconstructive/augmentation) surgeries to provide body mass and structural/mechanical support.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(937)847-8400orders@x-spine.com

Regulatory Flags#

DUNS number
081224143
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

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