FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

ALLOFIT ACETABULAR SYSTEM

K Number: K003758 · Decision Mar 7, 2001
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
113
Applicant Total
45
Review Days
91

Basic Information

Device Name
ALLOFIT ACETABULAR SYSTEM
K Number
K003758
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3330
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SULZER ORTHOPEDICS, INC.
Date Received
December 6, 2000
Decision Date
March 7, 2001
Product Code
KWA
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
KWA Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)

Similar 510(k) Clearances

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

View all

Other Clearances by SULZER ORTHOPEDICS, INC.

K Number Device Name
K022985 ASCENDENT ACETABULAR SYSTEM
K021578 NATURAL-KNEE II SYSTEM COCR TIBIAL BASEPLATE
K020713 MS-30 LATERAL FEMORAL STEM
K013935 ALLOFIT ACETABULAR SYSTEM 32MM ALPHA DURASUL INSERTS
K013031 MOST OPTIONS SYSTEM
K012739 CONVERGE ACETABULAR SYSTEM
K012961 SULZER ORTHOPEDICS CONVERGE ACETABULAR SYSTEM
K011954 SULZER ORTHOPEDICS ALLEGRETTO UNICOMPARTMENTAL KNEE
K010839 CLS VARUS STEM/CLS 135 STEM
K003801 ANATOMICAL PRESS-FIT HUMERAL STEM
Search all 45 clearances from SULZER ORTHOPEDICS, INC. →