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

OSTEO AUSTIN MOORE ENDOPROSTHESIS SYSTEM

K Number: K974807 · Decision Mar 16, 1998
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
106
Applicant Total
178
Review Days
83

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Basic Information

Device Name
OSTEO AUSTIN MOORE ENDOPROSTHESIS SYSTEM
K Number
K974807
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteonics Corp.
Date Received
December 23, 1997
Decision Date
March 16, 1998
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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K984585 OSTEONICS +10 UNIPOLAR ADAPTOR SLEEVE
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K990158 OSTEONICS COMBINATION SCREW RING/BLOCKER
K984302 OSTEONICS SPINAL SYSTEM CYLINDRICAL BONE SCREWS
K984353 OSTEO 9MM IC TIBIAL NAIL
K983502 OSTEONICS SECUR-FIT AD GENERATION II ACETABULAR COMPONENT SYSTEM
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