FDA UDI In Commercial Distribution 🇺🇸 United States

CoRoent

DI: 00887517673176 · Model: 1662613 · Nuvasive, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CoRoent
Primary DI
00887517673176
Version / Model
1662613
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-23
Public Version
8
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
f5435c9d-a20c-4230-ac3c-67a893434d7f

Device Description

CoRoent® SI Screw, 13x4.0mm Self-Drill

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
OVE Intervertebral fusion device with integrated fixation, cervical
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 00887517673176

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K142299 000
K161442 000
K170961 000
K192582 000
K231735 000