FDA UDI In Commercial Distribution 🇺🇸 United States

SP-FIX

DI: 00849044092363 · Model: 588.129 · GLOBUS MEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SP-FIX
Primary DI
00849044092363
Version / Model
588.129
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-07
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
97b6b161-f102-4a51-ab29-849bd91f2611

Device Description

SP-Fix Set Screw Locking Plate, 29mm

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
PEK Spinous process plate
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

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

Identifiers

Type ID
Primary 00849044092363

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K132191 000

Device Sizes

Type Value Unit Text
Length 29 Millimeter