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

BERLIN EXTERNAL FIXATOR

K Number: K954053 · Decision May 16, 1996
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
56
Applicant Total
85
Review Days
261

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Basic Information

Device Name
BERLIN EXTERNAL FIXATOR
K Number
K954053
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Encore Orthopedics, Inc.
Date Received
August 29, 1995
Decision Date
May 16, 1996
Product Code
LXT
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
LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite

Similar 510(k) Clearances

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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
Search all 85 clearances from Encore Orthopedics, Inc. →