FDA UDI In Commercial Distribution 🇺🇸 United States

ASTRA-OCT Spine System

DI: M824A3P35181 · Model: A3P-3518 · SPINECRAFT, LLC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ASTRA-OCT Spine System
Primary DI
M824A3P35181
Version / Model
A3P-3518
Catalog Number
A3P-3518
Company Name
SPINECRAFT, LLC
Labeler DUNS
783908713
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-03
Public Version
1
Public Version Date
2018-11-05
Public Version Status
New
Public Device Record Key
9024ab9d-089a-43f3-a752-72d16c8258a0

Device Description

ASTRA-OCT Dia. 3.5mm Polyaxial Screw, 18mm

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
Yes
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
NKG Orthosis, cervical pedicle screw spinal fixation

GMDN Terms

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

Identifiers

Type ID
Secondary 00193082079443
Primary M824A3P35181

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K181350 000