FDA UDI In Commercial Distribution 🇺🇸 United States

Revolution

DI: 00814033020177 · Model: 11655504 · INTELLIGENT IMPLANT SYSTEMS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Revolution
Primary DI
00814033020177
Version / Model
11655504
Catalog Number
11655504
Company Name
INTELLIGENT IMPLANT SYSTEMS, LLC
Labeler DUNS
013742030
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-14
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
09a00912-a195-4385-8263-284bb303bcc8

Device Description

5.5 X 50mm Cannulated Bone Screw, 4mm Offset

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00814033020177

Customer Contacts

Phone
704-424-1009

Premarket Submissions

Submission Number Supplement Number
K142939 000