FDA UDI In Commercial Distribution 🇺🇸 United States

PICASSO II

DI: 00841732124103 · Model: 119.2080 · CTL MEDICAL CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PICASSO II
Primary DI
00841732124103
Version / Model
119.2080
Company Name
CTL MEDICAL CORPORATION
Labeler DUNS
080138504
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-07
Public Version
1
Public Version Date
2023-09-15
Public Version Status
New
Public Device Record Key
9a7e646a-e60e-4b2e-9f53-ae7bc2b98ee6

Device Description

PICASSO™ II Percutaneous Polyaxial Screw, Semi-Closed 127mm, D9.5xL80mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

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

Identifiers

Type ID
Primary 00841732124103

Premarket Submissions

Submission Number Supplement Number
K140219 000