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

CCG CERCLAGE SYSTEM

K Number: K932024 · Decision Feb 14, 1995
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
128
Applicant Total
85
Review Days
659

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Basic Information

Device Name
CCG CERCLAGE SYSTEM
K Number
K932024
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Encore Orthopedics, Inc.
Date Received
April 26, 1993
Decision Date
February 14, 1995
Product Code
JDQ
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
JDQ Cerclage, Fixation

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Other Clearances by Encore Orthopedics, Inc.

K Number Device Name
K032905 3DKNEE POROUS COATED FEMORAL COMPONENT
K020114 3D KNEE
K020741 UNICONDYLAR KNEE
K020236 MODIFICATION TO PASS SPINAL SYSTEM
K020170 KEYSTONE HIP SYSTEM CALCAR REPLACEMENT BODY AND BUILD UP
K013490 CEMENTED CALCAR HIP SYSTEM
K013442 PASS SPINAL SYSTEM
K003324 PLASMA SPRAYED SHOULDER
K013431 PASS SPINAL SYSTEM
K013191 PASS SPINAL SYSTEM
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