FDA UDI Not in Commercial Distribution 🇺🇸 United States

Integrated Spine System

DI: 00822409030644 · Model: 158-4740-01 · Ortho Development Corporation
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Integrated Spine System
Primary DI
00822409030644
Version / Model
158-4740-01
Company Name
Ortho Development Corporation
Labeler DUNS
876542390
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
cf743a34-4506-4b4f-bd4e-01cd300a633a
Distribution End Date
2016-09-24

Device Description

Diameter 4.75 x 40 mm Pedicle 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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
MNI ORTHOSIS, SPINAL PEDICLE FIXATION

GMDN Terms

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

Identifiers

Type ID
Primary 00822409030644

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K061524 000

Device Sizes

Type Value Unit Text
Length 40 Millimeter
Outer Diameter 4.75 Millimeter