FDA UDI In Commercial Distribution 🇺🇸 United States

Palisade Pedicular Fixation System

DI: M7406706050 · Model: 10-10-59-17 · SPINEOLOGY INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Palisade Pedicular Fixation System
Primary DI
M7406706050
Version / Model
10-10-59-17
Catalog Number
670-6050
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-01
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
3ae5c68e-f26f-4603-be73-5b0ad2bf30a6

Device Description

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

GMDN Terms

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

Identifiers

Type ID
Primary M7406706050

Customer Contacts

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

Premarket Submissions

Submission Number Supplement Number
K153323 000

Device Sizes

Type Value Unit Text
Length 50 Millimeter
Device Size Text, specify 50