FDA UDI In Commercial Distribution 🇺🇸 United States

Paeon Posterior Cervical Fixation System

DI: 00840273306993 · Model: 6117-3540 · Aegis Spine, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Paeon Posterior Cervical Fixation System
Primary DI
00840273306993
Version / Model
6117-3540
Catalog Number
6117-3540
Company Name
Aegis Spine, Inc.
Labeler DUNS
017993061
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-27
Public Version
1
Public Version Date
2022-05-05
Public Version Status
New
Public Device Record Key
a60ed0fe-c8c9-4bfa-9aa1-65f01e36af8d

Device Description

Cervical Partially Polyaxial Screw Ø3.5x40mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
NKG Posterior Cervical Screw System

GMDN Terms

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

Identifiers

Type ID
Primary 00840273306993

Premarket Submissions

Submission Number Supplement Number
K210035 000