FDA UDI In Commercial Distribution 🇺🇸 United States

Capture Facet Screw System

DI: M7405205330 · Model: 10-10-45-9 · SPINEOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Capture Facet Screw System
Primary DI
M7405205330
Version / Model
10-10-45-9
Catalog Number
520-5330
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-08
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
02ac5910-c7c3-4eb9-b63a-75a63d2b785f

Device Description

Capture Facet Screw

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
MR Unsafe
Direct Marking Exempt
Yes
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
MRW SYSTEM, FACET SCREW SPINAL DEVICE

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary M7405205330

Customer Contacts

Phone
+1(651)256-8500 ext. 534

Device Sizes

Type Value Unit Text
Length 30 Millimeter
Device Size Text, specify 5.25 x 30