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

Univers Revers Humeral Cup Implant

K Number: K221232 · Decision May 19, 2022
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
70
Applicant Total
110
Review Days
20

Basic Information

Device Name
Univers Revers Humeral Cup Implant
K Number
K221232
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3690
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex Inc.
Date Received
April 29, 2022
Decision Date
May 19, 2022
Product Code
HSD
Advisory Committee
Orthopedic
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
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HSD), 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. →