FDA UDI In Commercial Distribution 🇺🇸 United States

InterPlate®

DI: 00817893021919 · Model: L-Ti · RSB SPINE LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
InterPlate®
Primary DI
00817893021919
Version / Model
L-Ti
Catalog Number
RSB514
Company Name
RSB SPINE LLC
Labeler DUNS
038558909
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2018-10-05
Public Version Status
Update
Public Device Record Key
bf9680b5-c6be-4dbd-9f3f-88b02ef0486c

Device Description

BONE SCREW EXTRACTOR

Device Characteristics

Single Use
No
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
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
HWB Extractor

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary 00817893021919

Premarket Submissions

Submission Number Supplement Number
K071922 000