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

EPSILON METASUL 32MM ACETABULAR INSERTS, STANDARD AND HOODED

K Number: K033634 · Decision Sep 15, 2004
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
113
Applicant Total
10
Review Days
301

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Basic Information

Device Name
EPSILON METASUL 32MM ACETABULAR INSERTS, STANDARD AND HOODED
K Number
K033634
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3330
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Centerpulse Orthopedics, Inc.
Date Received
November 19, 2003
Decision Date
September 15, 2004
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.

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Other Clearances by Centerpulse Orthopedics, Inc.

K Number Device Name
K033943 ALPHA METASUL 28MM AND 32MM ACETABULAR INSERTS, STANDARD AND HOODED
K040947 DURASUL BIPOLAR
K033810 NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM
K033664 MODIFICATION TO ALLOCLASSIC ZWEYMULLER SL OFFSET FEMORAL STEM
K032348 CONVERGE RETI-LOCK MULTI-HOLE REINFORCEMENT CUP
K030923 EPSILON DURASUL CONSTRAINED ACETABULAR LINER
K032380 WAGNER CONE PROSTHESIS
K031183 TIBIAL SPACER FOR THE NATURAL-KNEE II CEMENTED MODULAR TIBIAL BASEPLATE
K030373 ALLOCLASSIC ZWEYMUELLER SL/SLL FEMORAL STEM