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

7000 SERIES MODULAR TIBIAL COMPONENTS

K Number: K915192 · Decision Feb 14, 1992
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
178
Review Days
87

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Basic Information

Device Name
7000 SERIES MODULAR TIBIAL COMPONENTS
K Number
K915192
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Osteonics Corp.
Date Received
November 19, 1991
Decision Date
February 14, 1992
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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K982798 OSTEONICS ANTERIOR CERVICAL COMPRESSION PLATING SYSTEM
K984585 OSTEONICS +10 UNIPOLAR ADAPTOR SLEEVE
K990203 OSTEONICS PRIMARY SECUR-FIT PLUS HIP STEMS
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
Search all 178 clearances from Osteonics Corp. →