FDA UDI In Commercial Distribution 🇺🇸 United States

PLS

DI: G463066393BK0 · Model: 06.6393B-K · BOXSPINE HOLDINGS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PLS
Primary DI
G463066393BK0
Version / Model
06.6393B-K
Catalog Number
06.6393B-K
Company Name
BOXSPINE HOLDINGS, INC.
Labeler DUNS
126547906
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-12
Public Version
1
Public Version Date
2025-06-20
Public Version Status
New
Public Device Record Key
53b34c9a-b63d-4a9e-9520-e1812f206a05

Device Description

Ø5.5 Polyaxial Pedicle Screw Non-Cannulated with Screw Cap Ø7.5 x 35mm (Violet)

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
KWP Appliance, Fixation, Spinal Interlaminal
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary G463066393BK0