Medical Device Manufacturer · US , Austin , TX

Centerpulse Orthopedics, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2003

Total

Cleared

Denied

Centerpulse Orthopedics, Inc. has 10 FDA 510(k) cleared orthopedic devices. Based in Austin, US.

Historical record: 10 cleared submissions from 2003 to 2004.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Centerpulse Orthopedics, Inc.

10 devices

1-10 of 10

Cleared Oct 18, 2004

ALPHA METASUL 28MM AND 32MM ACETABULAR INSERTS, STANDARD AND HOODED

K033943 · KWA

Orthopedic · 304d

Cleared Sep 15, 2004

EPSILON METASUL 32MM ACETABULAR INSERTS, STANDARD AND HOODED

NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM

K033810 · HRY

Orthopedic · 88d

Cleared Dec 17, 2003

MODIFICATION TO ALLOCLASSIC ZWEYMULLER SL OFFSET FEMORAL STEM

K033664 · LZO

Orthopedic · 26d

Cleared Oct 24, 2003

CONVERGE RETI-LOCK MULTI-HOLE REINFORCEMENT CUP

K032348 · LZO

Orthopedic · 86d

Cleared Oct 03, 2003

EPSILON DURASUL CONSTRAINED ACETABULAR LINER

K030923 · KWZ

Orthopedic · 193d

Cleared Sep 22, 2003

WAGNER CONE PROSTHESIS

K032380 · LZO

Orthopedic · 52d

Cleared Jul 14, 2003

TIBIAL SPACER FOR THE NATURAL-KNEE II CEMENTED MODULAR TIBIAL BASEPLATE

K031183 · JWH

Orthopedic · 90d

Cleared Mar 06, 2003

ALLOCLASSIC ZWEYMUELLER SL/SLL FEMORAL STEM

K030373 · LZO

Orthopedic · 30d

Centerpulse Orthopedics, Inc. - FDA 510(k) Cleared Devices

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