FDA UDI In Commercial Distribution 🇺🇸 United States

Nautilus Spinal System

DI: 00190837057329 · Model: 385-65-5 · Life Spine, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Nautilus Spinal System
Primary DI
00190837057329
Version / Model
385-65-5
Catalog Number
385-65-5
Company Name
Life Spine, Inc.
Labeler DUNS
183641617
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-07
Public Version
1
Public Version Date
2019-11-15
Public Version Status
New
Public Device Record Key
2a7d1bf6-a99f-43e0-8249-8752f298a4b7

Device Description

Nautilus Assembly CA, Ø8.5 x 65 Long x 5 Lead

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
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

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

Identifiers

Type ID
Primary 00190837057329

Premarket Submissions

Submission Number Supplement Number
K111953 000