Medical Device Manufacturer · US , San Diego , CA

Sutter Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1989

7

Total

7

Cleared

0

Denied

Sutter Corp. has 7 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 7 cleared submissions from 1989 to 1995. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Sutter Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sutter Corp.

7 devices

1-7 of 7

Cleared Jun 12, 1995

SUTTER HAMMERTOE JOINT PROSTHESIS

Orthopedic · 335d

Cleared Feb 27, 1995

SUTTER MODEL 6000 HAND CPM DEVICE

Physical Medicine · 124d

Cleared Mar 10, 1994

SUTTER PROXIMAL INTERPHALANGEAL JOINT

Orthopedic · 344d

Cleared Feb 22, 1993

FIRST METATARSOPHALANGEAL JOINT MOTION SPLINT

Physical Medicine · 160d

Cleared Jan 08, 1992

SUTTER MODEL 10000 LEG CPM DEVICE

Physical Medicine · 71d

Cleared Jul 25, 1990

MODEL 9000 AT ANKLE CPM DEVICE

Physical Medicine · 36d

Cleared Feb 27, 1989

SUTTER HOSPITAL CPM

Physical Medicine · 21d