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

OVOMotion Reverse Shoulder Arthroplasty System

K Number: K203375 · Decision Jun 24, 2021
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
203
Applicant Total
26
Review Days
220

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Basic Information

Device Name
OVOMotion Reverse Shoulder Arthroplasty System
K Number
K203375
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrosurface, Inc.
Date Received
November 16, 2020
Decision Date
June 24, 2021
Product Code
PHX
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
PHX Shoulder Prosthesis, Reverse Configuration

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Other Clearances by Arthrosurface, Inc.

K Number Device Name
K200718 Arthrosurface WristMotion Total Wrist Arthroplasty System
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K181280 Patello-Femoral Wave (Kahuna) Arthroplasty System
K173964 OVOMotion Shoulder Arthroplasty System
K172383 Arthrosurface Bone Screws
K170440 KISSloc Suture System
K170350 ToeMATE® Hammertoe Correction System
K162391 AlignMATE™ Lapidus Arthrodesis System
K161539 Arthrosurface Bone Screws
K152454 HemiCAP MTP Resurfacing Hemi-Arthroplasty System
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