FDA UDI In Commercial Distribution 🇺🇸 United States

AttraX

DI: 00887517939968 · Model: 5015120 · Nuvasive, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AttraX
Primary DI
00887517939968
Version / Model
5015120
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-05
Public Version
4
Public Version Date
2023-07-12
Public Version Status
Update
Public Device Record Key
76c19069-6ab2-43ea-8a62-8df127f73b9a

Device Description

AttraX® Scaffold Morsels, 20cc

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQV FILLER, BONE VOID, CALCIUM COMPOUND

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 00887517939968

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K090641 000
K151584 000
K172497 000
K191974 000