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

H-MAX S FEMORAL STEMS, MODULAR FEMORAL HEADS, CEMENTED CUPS, LOCK BIPOLAR HEADS

K Number: K112091 · Decision Nov 9, 2012
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
157
Applicant Total
23
Review Days
477

Basic Information

Device Name
H-MAX S FEMORAL STEMS, MODULAR FEMORAL HEADS, CEMENTED CUPS, LOCK BIPOLAR HEADS
K Number
K112091
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LIMACORPORATE S.P.A.
Date Received
July 21, 2011
Decision Date
November 9, 2012
Product Code
MEH
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
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

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