FDA UDI In Commercial Distribution 🇺🇸 United States

Ibis

DI: 00822409019342 · Model: 158-0130-03A · Ortho Development Corporation
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ibis
Primary DI
00822409019342
Version / Model
158-0130-03A
Company Name
Ortho Development Corporation
Labeler DUNS
876542390
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d58156fd-5323-4459-b2bf-d6e080628589

Device Description

Diameter 5.5 mm x 130 mm Curved Bulleted Rod Ti

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

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

Identifiers

Type ID
Primary 00822409019342

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K142146 000

Device Sizes

Type Value Unit Text
Length 130 Millimeter
Outer Diameter 5.5 Millimeter