FDA UDI In Commercial Distribution 🇺🇸 United States

Threshold Curved Rod

DI: M7405302075 · Model: 10-10-07-33 · SPINEOLOGY INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Threshold Curved Rod
Primary DI
M7405302075
Version / Model
10-10-07-33
Catalog Number
530-2075
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-03-30
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d2fb7cf4-6484-4bc6-b94d-343a51c64bd4

Device Description

Curved Rod

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
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
MNH Orthosis, spondylolisthesis spinal fixation
MNI ORTHOSIS, SPINAL PEDICLE FIXATION

GMDN Terms

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

Identifiers

Type ID
Primary M7405302075

Customer Contacts

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

Premarket Submissions

Submission Number Supplement Number
K143403 000

Device Sizes

Type Value Unit Text
Length 75 Millimeter
Device Size Text, specify 5.5x75