FDA UDI In Commercial Distribution 🇺🇸 United States

CoRoent

DI: 00887517818003 · Model: 1835710 · Nuvasive, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CoRoent
Primary DI
00887517818003
Version / Model
1835710
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-09
Public Version
6
Public Version Date
2021-04-21
Public Version Status
Update
Public Device Record Key
5d5f86b2-59cc-4594-a363-a6bdde5183e9

Device Description

CoRoent Contour Trial Drill Guide, S10

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
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
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 00887517818003

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K163491 000