510(k) K230904

Device
Arthrex Virtual Implant Positioning (VIP) System
Applicant
Arthrex, Inc.
510(k) number
K230904
Product code
QHE
Decision
Substantially Equivalent (SESE)
Decision date
2023-06-22
Date received
2023-03-31
Regulation
888.3660
Classification name
Shoulder Arthroplasty Implantation System
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Troy Brooks
Address
1370 Creekside Blvd. Naples FL US 34108 34108

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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