FDA UDI In Commercial Distribution 🇺🇸 United States

PEEK PREVAIL™ Cervical Interbody Device

DI: 00613994753922 · Model: 1225555 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PEEK PREVAIL™ Cervical Interbody Device
Primary DI
00613994753922
Version / Model
1225555
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
5
Public Version Date
2020-04-06
Public Version Status
Update
Public Device Record Key
96653e5a-0ae2-4fd1-b1d6-8b9d1e5f62a7

Device Description

SCREW GUIDE 1225555

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OVE Intervertebral fusion device with integrated fixation, cervical

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 00613994753922

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K113252 000