FDA UDI In Commercial Distribution 🇺🇸 United States

Stainless Steel

DI: 10889981024956 · Model: 25-32-4050 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Stainless Steel
Primary DI
10889981024956
Version / Model
25-32-4050
Catalog Number
25-32-4050
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
393c0160-279b-4b49-b5d2-b31f3c2c7df0

Device Description

Polyaxial Reduction Screw, SS, 4.00mm x 50mm

Device Characteristics

Single Use
No
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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
MNH Orthosis, spondylolisthesis spinal fixation
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
MNI ORTHOSIS, SPINAL PEDICLE FIXATION

GMDN Terms

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

Identifiers

Type ID
Primary 10889981024956

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120829 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 4.00mm x 50mm