FDA UDI Not in Commercial Distribution 🇺🇸 United States

Stainless Steel

DI: 10381780029601 · Model: 25-15-4050 · INTEGRA LIFESCIENCES CORPORATION
Product Codes
5
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Stainless Steel
Primary DI
10381780029601
Version / Model
25-15-4050
Catalog Number
25-15-4050
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
6b2d049f-e84f-4caa-94e2-f4636170bc37
Distribution End Date
2015-11-15

Device Description

D-Planar Screw, 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
MNH Orthosis, Spondylolisthesis Spinal Fixation
KWQ Appliance, Fixation, Spinal Intervertebral Body
MNI Orthosis, Spinal Pedicle Fixation
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

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

Identifiers

Type ID
Secondary M248251540501
Primary 10381780029601

Customer Contacts

Device Sizes

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