FDA UDI Not in Commercial Distribution 🇺🇸 United States

VSP

DI: 10705034240992 · Model: 22263250F · DEPUY SPINE, LLC
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VSP
Primary DI
10705034240992
Version / Model
22263250F
Catalog Number
22263250F
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
5
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
17ea3aa2-98a2-4549-a692-2587a3dd5b90
Distribution End Date
2018-06-20

Device Description

VSP SPINE SYSTEM BONE SCREW WITH FLUTED END 7.0 x 50mm

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
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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 10705034240992

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K980485 000