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

Trinity PLUS Acetabular Shell

K Number: K172551 · Decision Jun 15, 2018
Classifications
1
FEI Numbers
271
Registration Numbers
271
Same Product Code
551
Applicant Total
18
Review Days
296

Basic Information

Device Name
Trinity PLUS Acetabular Shell
K Number
K172551
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Corin USA Limited
Date Received
August 23, 2017
Decision Date
June 15, 2018
Product Code
LPH
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
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

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