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

HOWMEDICA STRAIGHT STEM FEMORAL COMPONENT

K Number: K940307 · Decision Jan 19, 1995
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
36
Review Days
360

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Basic Information

Device Name
HOWMEDICA STRAIGHT STEM FEMORAL COMPONENT
K Number
K940307
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica, Inc.
Date Received
January 24, 1994
Decision Date
January 19, 1995
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

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Other Clearances by Howmedica, Inc.

K Number Device Name
K984251 XIA SPINE SYSTEM
K984202 HOWMEDICA HUMERAL INTERCALARY SYSTEM
K984305 ZETA MULTIZONE LOCKING NAIL SYSTEM
K983885 BURR HOLE COVERS, CRANIOMAXILLOFACIAL PLATES
K983358 G/K SFN AND STN LOCKING NAILS
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
K980843 EXETER INTRAMEDULLARY BONE PLUG
Search all 36 clearances from Howmedica, Inc. →