Medical Device Manufacturer · US , Austin , TX

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

45 submissions · 41 cleared · Since 1997
45
Total
41
Cleared
0
Denied

Sulzer Orthopedics, Inc. has 41 FDA 510(k) cleared orthopedic devices. Based in Austin, US.

Historical record: 41 cleared submissions from 1997 to 2002.

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 - Sulzer Orthopedics, Inc.
45 devices
1-12 of 45
Cleared Dec 05, 2002
ASCENDENT ACETABULAR SYSTEM
K022985 · LZO
Orthopedic · 87d
Cleared Aug 09, 2002
NATURAL-KNEE II SYSTEM COCR TIBIAL BASEPLATE
K021578 · JWH
Orthopedic · 87d
Cleared May 14, 2002
MS-30 LATERAL FEMORAL STEM
K020713 · LZO
Orthopedic · 70d
Cleared Dec 13, 2001
ALLOFIT ACETABULAR SYSTEM 32MM ALPHA DURASUL INSERTS
K013935 · LZO
Orthopedic · 15d
Cleared Dec 07, 2001
MOST OPTIONS SYSTEM
K013031 · KRO
Orthopedic · 88d
Cleared Nov 14, 2001
CONVERGE ACETABULAR SYSTEM
K012739 · LPH
Orthopedic · 90d
Cleared Oct 18, 2001
SULZER ORTHOPEDICS CONVERGE ACETABULAR SYSTEM
K012961 · JDI
Orthopedic · 44d
Cleared Sep 19, 2001
SULZER ORTHOPEDICS ALLEGRETTO UNICOMPARTMENTAL KNEE
K011954 · HSX
Orthopedic · 89d
Cleared Apr 18, 2001
CLS VARUS STEM/CLS 135 STEM
K010839 · LZO
Orthopedic · 28d
Cleared Mar 07, 2001
ALLOFIT ACETABULAR SYSTEM
K003758 · KWA
Orthopedic · 91d
Cleared Feb 28, 2001
ANATOMICAL PRESS-FIT HUMERAL STEM
K003801 · KWS
Orthopedic · 82d
Cleared Jan 04, 2001
UNICONDYLAR INTERPOSITIONAL SPACER
K003269 · HSH
Orthopedic · 78d

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