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

ANATOMICAL SHOULDER FRACTURE SYSTEM

K Number: K062029 · Decision Oct 31, 2006
Classifications
1
FEI Numbers
218
Registration Numbers
218
Same Product Code
189
Applicant Total
43
Review Days
105

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Basic Information

Device Name
ANATOMICAL SHOULDER FRACTURE SYSTEM
K Number
K062029
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer GmbH
Date Received
July 18, 2006
Decision Date
October 31, 2006
Product Code
KWS
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
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

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