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

BDH UNIPOLAR FEMORAL COMPONENT A2

K Number: K833403 · Decision Jan 10, 1984
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
106
Applicant Total
22
Review Days
102

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Basic Information

Device Name
BDH UNIPOLAR FEMORAL COMPONENT A2
K Number
K833403
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Carbomedics, Inc.
Date Received
September 30, 1983
Decision Date
January 10, 1984
Product Code
KWL
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
KWL Prosthesis, Hip, Hemi-, Femoral, Metal

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