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

HUMELOCK CEMENTED SHOULDER PROSTHESIS

K Number: K111097 · Decision Nov 9, 2011
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
70
Applicant Total
8
Review Days
203

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Basic Information

Device Name
HUMELOCK CEMENTED SHOULDER PROSTHESIS
K Number
K111097
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3690
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fx Solutions
Date Received
April 20, 2011
Decision Date
November 9, 2011
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.

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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
K140071 HUMELOCK II CEMENTED SHOULDER SYSTEM
K130759 HUMELOCK II CEMENTLESS SHOULDER SYSTEM
K123814 HUMELOCK II CEMENTED SHOULDER SYSTEM