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

OMNIFLEX NORMALIZED HIP STEM FOR PRESS-FIT FIXAT.

K Number: K872768 · Decision Jan 14, 1988
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
113
Applicant Total
178
Review Days
184

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Basic Information

Device Name
OMNIFLEX NORMALIZED HIP STEM FOR PRESS-FIT FIXAT.
K Number
K872768
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3330
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Osteonics Corp.
Date Received
July 14, 1987
Decision Date
January 14, 1988
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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