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

P.C.A. E-SERIES HIP- CEMENTLESS USE

K Number: K945093 · Decision Jan 19, 1995
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
36
Review Days
94

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Basic Information

Device Name
P.C.A. E-SERIES HIP- CEMENTLESS USE
K Number
K945093
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Howmedica, Inc.
Date Received
October 17, 1994
Decision Date
January 19, 1995
Product Code
LZO
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

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Other Clearances by Howmedica, Inc.

K Number Device Name
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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. →