FDA UDI Not in Commercial Distribution 🇺🇸 United States

UCR

DI: 10381780000808 · Model: 11-5555 · Seaspine, Inc.
Product Codes
4
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
UCR
Primary DI
10381780000808
Version / Model
11-5555
Catalog Number
11-5555
Company Name
Seaspine, Inc.
Labeler DUNS
119614407
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-18
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
31cd1638-e778-499c-9303-e749ac90ec0b
Distribution End Date
2015-11-15

Device Description

Polyaxial Reduction Screw 5.5 x 55 mm

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
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

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

Identifiers

Type ID
Secondary M5561155551
Primary 10381780000808

Device Sizes

Type Value Unit Text
Device Size Text, specify 5.5 x 55 mm