FDA UDI In Commercial Distribution 🇺🇸 United States

Armada

DI: 00887517285386 · Model: 8531570 · Nuvasive, Inc.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Armada
Primary DI
00887517285386
Version / Model
8531570
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-04
Public Version
1
Public Version Date
2019-12-12
Public Version Status
New
Public Device Record Key
0f004ba0-e256-4255-a8ea-a5945dec7a0c

Device Description

ARM15S Screw, 10.5x70mm Iliac SL-Closed

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
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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNI Orthosis, spinal pedicle fixation
NKB Thoracolumbosacral pedicle screw system
MNH Orthosis, spondylolisthesis spinal fixation
KWQ Appliance, fixation, spinal intervertebral body

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00887517285386

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K092287 000