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

OsseoFit Stemless Shoulder System

K Number: K241873 · Decision Dec 11, 2024
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
18
Applicant Total
376
Review Days
167

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Basic Information

Device Name
OsseoFit Stemless Shoulder System
K Number
K241873
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer, Inc.
Date Received
June 27, 2024
Decision Date
December 11, 2024
Product Code
PKC
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
PKC Prosthesis, Total Anatomic Shoulder, Uncemented Metaphyseal Humeral Stem With No Diaphyseal Incursion, Semi-Constrained

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