FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

ZIMMER MMC CUP

K Number: K091003 · Decision Nov 24, 2009
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
113
Applicant Total
43
Review Days
230

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Basic Information

Device Name
ZIMMER MMC CUP
K Number
K091003
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3330
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer GmbH
Date Received
April 8, 2009
Decision Date
November 24, 2009
Product Code
KWA
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
KWA Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)

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