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

PARTNERSHIP CALCAR FEMORAL COMPONENTS

K Number: K980239 · Decision Apr 16, 1998
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
36
Review Days
83

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PARTNERSHIP CALCAR FEMORAL COMPONENTS
K Number
K980239
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica, Inc.
Date Received
January 23, 1998
Decision Date
April 16, 1998
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LZO), ordered by most recent decision date.

View all

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. →