Medical Device Manufacturer · US , Rancho Cordova , CA

Synvasive Technology, Inc. - FDA 510(k) Cleared Devices

10 submissions · 9 cleared · Since 1994

Total

Cleared

Denied

Synvasive Technology, Inc. has 9 FDA 510(k) cleared orthopedic devices. Based in Rancho Cordova, US.

Historical record: 9 cleared submissions from 1994 to 2011.

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 - Synvasive Technology, Inc.

10 devices

1-10 of 10

Cleared Mar 22, 2011

ELIBRA UNI SOFT-TISSUE FORCE SENSOR, MODEL 61-XXXX(5 MODELS, DIFFERENT SIZES

K093046 · ONN

Orthopedic · 538d

Cleared Apr 04, 2007

ELIBRA DYNAMIC KNEE BALANCER

K070108 · ONN

Orthopedic · 83d

Cleared Aug 26, 1997

SURGICAL BURS AND SURGICAL DRILL BITS

K972508 · HWE

Orthopedic · 54d

Cleared Sep 23, 1996

KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN

K961522 · HTY

Orthopedic · 154d

Cleared Aug 18, 1995

POWERGRIP(TM) COMPRESSION FIXATION DEVICE

General & Plastic Surgery · 247d

Cleared Apr 07, 1994

SYNVASIVE CERAMIC SUTTING BLOCK

HEDLEYL INTRAMEDULLARY PREPARATION BRUSH

K931737 · HTZ

General & Plastic Surgery · 275d

Synvasive Technology, Inc. - FDA 510(k) Cleared Devices

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