FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

HUMELOCK II CEMENTED SHOULDER SYSTEM

K Number: K140071 · Decision Jul 28, 2014
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
70
Applicant Total
8
Review Days
196

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Basic Information

Device Name
HUMELOCK II CEMENTED SHOULDER SYSTEM
K Number
K140071
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3650
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fx Solutions
Date Received
January 13, 2014
Decision Date
July 28, 2014
Product Code
KWT
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
KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KWT), ordered by most recent decision date.

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Other Clearances by Fx Solutions

K Number Device Name
K163669 Humeris Shoulder
K162455 Humelock Reversed Shoulder
K150488 Humelock II Reversible Shoulder System
K143721 PRCT2
K130759 HUMELOCK II CEMENTLESS SHOULDER SYSTEM
K123814 HUMELOCK II CEMENTED SHOULDER SYSTEM
K111097 HUMELOCK CEMENTED SHOULDER PROSTHESIS