FDA UDI In Commercial Distribution 🇺🇸 United States

CAPTURE

DI: M7404105335 · Model: 70-01-002-3 · SPINEOLOGY INC.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
CAPTURE
Primary DI
M7404105335
Version / Model
70-01-002-3
Catalog Number
410-5335
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-05
Public Version
4
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
7aa3888f-69da-4a3e-a7df-25f4894c82af

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MRW System, Facet Screw Spinal Device
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary M7404105335

Customer Contacts

Phone
+1(612)256-8500 ext. 534

Device Sizes

Type Value Unit Text
Length 35 Millimeter
Device Size Text, specify 5.25x35