FDA UDI In Commercial Distribution 🇺🇸 United States

LAT-FUSE™* LATERAL PLATE SYSTEM

DI: 00846468014162 · Model: 38-SD65-46 · Pioneer Surgical Technology, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LAT-FUSE™* LATERAL PLATE SYSTEM
Primary DI
00846468014162
Version / Model
38-SD65-46
Catalog Number
38-SD65-46
Company Name
Pioneer Surgical Technology, Inc.
Labeler DUNS
793384496
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-01-13
Public Version
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
d229d140-bb46-4533-865c-5b20cfc832e8

Device Description

SELF-DRILLING SCREW

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
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00846468014162

Premarket Submissions

Submission Number Supplement Number
K120724 000