FDA UDI In Commercial Distribution 🇺🇸 United States

Cambria™

DI: 10889981058043 · Model: 93-9126 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cambria™
Primary DI
10889981058043
Version / Model
93-9126
Catalog Number
93-9126
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-22
Public Version
4
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
d00e8d71-327e-42f7-8b3a-eba35c6ff574

Device Description

Trial, Small w/ Stop 13mm x 12mm x 6mm

Device Characteristics

Single Use
No
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
No
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 10889981058043

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K082309 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 13mm x 12mm x 6mm