FDA UDI In Commercial Distribution 🇺🇸 United States

REVLOK

DI: 00889095222319 · Model: 178.383S · GLOBUS MEDICAL, INC.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REVLOK
Primary DI
00889095222319
Version / Model
178.383S
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-06
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
6ca43060-5186-461a-9d93-5d6955a1d734

Device Description

6.5mm REVLOK HA 5.5 Uniplanar 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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MNH Orthosis, spondylolisthesis spinal fixation
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
MNI ORTHOSIS, SPINAL PEDICLE 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 00889095222319

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K110280 000

Device Sizes

Type Value Unit Text
Outer Diameter 6.5 Millimeter
Length 40 Millimeter