FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ArthrexVIP Web Portal

K Number: K193523 · Decision Apr 30, 2020
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
110
Review Days
133

Basic Information

Device Name
ArthrexVIP Web Portal
K Number
K193523
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex Inc.
Date Received
December 19, 2019
Decision Date
April 30, 2020
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLZ System, Image Processing, Radiological

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LLZ), ordered by most recent decision date.

View all

Other Clearances by Arthrex Inc.

K Number Device Name
K251145 Arthrex PushLock Suture Anchors
K251453 Arthrex iBalance Partial Knee System
K243480 SuturePatch Tissue Reinforcement
K250596 Arthrex FiberTak Suture Anchor
K243995 Arthrex Humeral Plating System and Cerclage Button
K250424 Arthrex TightRope Soft Button, RT
K243344 Arthrex FiberTape and TigerTape Cerclage Sutures; Arthrex Radiopaque FiberTape Cerclage Sutures
K243742 Arthrex DynaNite Nitinol Staples
K243890 Arthrex Intramedullary Nails
K242079 Arthrex Elbow Fracture Plating System
Search all 110 clearances from Arthrex Inc. →