FDA UDI In Commercial Distribution 🇺🇸 United States

REVLOK

DI: 00889095222890 · Model: 178.509S · GLOBUS MEDICAL, INC.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REVLOK
Primary DI
00889095222890
Version / Model
178.509S
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
1cf2dd01-079f-4f8b-b5a5-223257e59bc7

Device Description

7.0mm REVLOK HA 5.5 DOD Polyaxial Screw, 75mm

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

GMDN Terms

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

Identifiers

Type ID
Primary 00889095222890

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K110280 000

Device Sizes

Type Value Unit Text
Length 75 Millimeter
Outer Diameter 7 Millimeter