FDA UDI In Commercial Distribution 🇺🇸 United States

ALLOMATRIX

DI: 00840420133502 · Model: 86XC0500 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ALLOMATRIX
Primary DI
00840420133502
Version / Model
86XC0500
Catalog Number
86XC0500
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
6
Public Version Date
2026-01-16
Public Version Status
Update
Public Device Record Key
b9205c30-2abd-4310-a605-6f26b8ba2c28

Device Description

Custom Bone Putty

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
Yes
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQV FILLER, BONE VOID, CALCIUM COMPOUND
MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)

GMDN Terms

Code Name
47257 Bone matrix implant, human-derived

Identifiers

Type ID
Primary 00840420133502

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 5 Milliliter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius