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

HOWMEDICA HUMERAL INTERCALARY SYSTEM

K Number: K984202 · Decision Feb 5, 1999
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
70
Applicant Total
36
Review Days
73

Basic Information

Device Name
HOWMEDICA HUMERAL INTERCALARY SYSTEM
K Number
K984202
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3690
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HOWMEDICA, INC.
Date Received
November 24, 1998
Decision Date
February 5, 1999
Product Code
HSD
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
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented

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K982463 EXTRACRANIAL RADIOTHERAPY SYSTEM
K982248 HOWMEDICA ASYMMETRIC STEM VITALOCK CLUSTER & SPIKED SHELLS, AND ACETABULAR SHELLS WITH MESH INGROWTH SURFACE WITH PERI-A
K980813 RELIANCE LONG STEM FEMORAL COMPONENTS
K981283 ROGACHEFSKY DISTAL RADIUS PLATES
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