Medical Device Manufacturer · US , Cupertino , CA

Novare Surgical Systems, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2000

Total

Cleared

Denied

Novare Surgical Systems, Inc. has 9 FDA 510(k) cleared medical devices. Based in Cupertino, US.

Historical record: 9 cleared submissions from 2000 to 2007. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Novare Surgical Systems, Inc. Filter by specialty or product code using the sidebar.

Novare Surgical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Novare Surgical Systems, Inc.

9 devices

1-9 of 9

Cleared Oct 16, 2007

REALHAND HIGH DEXTERITY INSTRUMENTS

K072715 · GCJ

General & Plastic Surgery · 21d

Cleared Jun 29, 2007

REALHAND HIGH DEXTERITY (HD) INSTRUMENTS

K071488 · GCJ

General & Plastic Surgery · 30d

Cleared Mar 10, 2005

ENDOLINK TRUE MOVEMENT SYSTEM

K043541 · GCJ

General & Plastic Surgery · 78d

Cleared Sep 05, 2003

ENCLOSE II ANASTOMOSIS ASSIST DEVICE

K032589 · DXC

Cardiovascular · 14d

Cleared Jan 16, 2003

ENCLOSE ANASTOMOSIS ASSIST DEVICE

Cardiovascular · 515d

Cleared Feb 11, 2002

INCLUDER CLAMP

K010694 · DXC

Cardiovascular · 340d

Cleared Jun 08, 2000

ENGAGE JAW INSERTS

K992980 · DXC

Cardiovascular · 279d

Novare Surgical Systems, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Novare Surgical Systems, Inc.

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