FDA UDI In Commercial Distribution 🇺🇸 United States

Cross Connector, Large

DI: M739247149750 · Model: 2471-4975 · CAPTIVA SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cross Connector, Large
Primary DI
M739247149750
Version / Model
2471-4975
Company Name
CAPTIVA SPINE, INC.
Labeler DUNS
836975784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
a8ad7bdb-c6de-47f4-b177-c60646cacc11

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
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
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation

GMDN Terms

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

Identifiers

Type ID
Primary M739247149750

Premarket Submissions

Submission Number Supplement Number
K120292 000