FDA UDI In Commercial Distribution 🇺🇸 United States

REVLOK

DI: 00889095224672 · Model: 178.766 · GLOBUS MEDICAL, INC.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REVLOK
Primary DI
00889095224672
Version / Model
178.766
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-07
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
0e5623af-f62b-46b7-9bfb-8e443794c48c

Device Description

6.5mm REVLOK 5.5 Uniplanar Reduction Screw, 40mm

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
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
MNH Orthosis, spondylolisthesis spinal fixation
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease

GMDN Terms

Code Name
37272 Trans-facet-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00889095224672

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K110280 000

Device Sizes

Type Value Unit Text
Length 40 Millimeter
Outer Diameter 6.5 Millimeter