FDA UDI In Commercial Distribution 🇺🇸 United States

APX

DI: 00887517210593 · Model: 1632872 · Nuvasive, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
APX
Primary DI
00887517210593
Version / Model
1632872
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-11
Public Version
1
Public Version Date
2023-07-19
Public Version Status
New
Public Device Record Key
ee1450d7-5a6d-4f0c-8295-b4263ba34bc5

Device Description

XLIF APX Template, 30x55mm

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
Yes
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
MAX Intervertebral fusion device with bone graft, lumbar
PHM Intervertebral fusion device with bone graft, thoracic

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 00887517210593

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K130820 000
K140770 000
K151374 000
K153105 000
K173025 000