FDA UDI In Commercial Distribution 🇺🇸 United States

XLIF

DI: 00887517804136 · Model: D6910018 · Nuvasive, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
XLIF
Primary DI
00887517804136
Version / Model
D6910018
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-21
Public Version
4
Public Version Date
2019-04-23
Public Version Status
Update
Public Device Record Key
c86a6b2b-0f31-4ed8-87e3-3b81f9add0fc

Device Description

ALBINS Inserter, 18mm Angled

Device Characteristics

Single Use
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
OVD Intervertebral fusion device with integrated fixation, lumbar
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00887517804136

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K161230 000