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

OMNIFIT(R) TOTAL KNEE SYSTEM (MODIFICATION)

K Number: K871769 · Decision Jun 2, 1987
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
178
Review Days
27

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Basic Information

Device Name
OMNIFIT(R) TOTAL KNEE SYSTEM (MODIFICATION)
K Number
K871769
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Osteonics Corp.
Date Received
May 6, 1987
Decision Date
June 2, 1987
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

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