FDA UDI In Commercial Distribution 🇺🇸 United States

HiJAK™ Cervical

DI: M68120190100170 · Model: 2019-01-0017 · ATLAS SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HiJAK™ Cervical
Primary DI
M68120190100170
Version / Model
2019-01-0017
Catalog Number
2019-01-0017
Company Name
ATLAS SPINE, INC.
Labeler DUNS
140801007
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-30
Public Version
2
Public Version Date
2020-09-07
Public Version Status
Update
Public Device Record Key
e7294f41-30b2-4269-923c-0c5a0af6c426

Device Description

20° Implant Inserter, HiJAK™ Cervical

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
MR Conditional
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary M68120190100170

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180675 000