FDA UDI In Commercial Distribution 🇺🇸 United States

Streamline® OCT Occipito-Cervico-Thoracic System

DI: 00846468077976 · Model: 23-CC-ROD-70 · Pioneer Surgical Technology, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Streamline® OCT Occipito-Cervico-Thoracic System
Primary DI
00846468077976
Version / Model
23-CC-ROD-70
Catalog Number
23-CC-ROD-70
Company Name
Pioneer Surgical Technology, Inc.
Labeler DUNS
793384496
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-10
Public Version
4
Public Version Date
2021-10-14
Public Version Status
Update
Public Device Record Key
abad90cd-c838-4a28-b12f-06a74924cb9c

Device Description

Straight Co-Cr Rod, 70mm length

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
KWP Appliance, Fixation, Spinal Interlaminal
NKG Orthosis, Cervical Pedicle Screw Spinal Fixation

GMDN Terms

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

Identifiers

Type ID
Primary 00846468077976

Premarket Submissions

Submission Number Supplement Number
K161498 000
K172139 000