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

BICON-PLUS ACETABULAR COMPONENTS

K Number: K992154 · Decision Apr 6, 2000
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
560
Applicant Total
38
Review Days
286

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Basic Information

Device Name
BICON-PLUS ACETABULAR COMPONENTS
K Number
K992154
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Plus Orthopedics
Date Received
June 25, 1999
Decision Date
April 6, 2000
Product Code
LPH
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
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LPH), ordered by most recent decision date.

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Other Clearances by Plus Orthopedics

K Number Device Name
K032126 PROMOS SHOULDER
K033763 MODIFICATION TO SLIM GLIDING NAIL SYSTEM
K032709 MODULAR PLUS HIP STEM
K032548 IP-XS COMPRESSION NAIL SYSTEM
K032215 VKS/TC-PLUS REVISION KNEE
K032052 UC-PLUS SOLUTION UNICONDYLAR KNEE
K031165 PLUS ORTHOPEDICS CEMENTED HIP STEM
K030971 MODIFICATION TO MODULAR PLUS REVISION STEM
K024134 UNI HIP STEM
K023667 RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEE
Search all 38 clearances from Plus Orthopedics →