Medical Device Manufacturer · US , Mchenry , IL

Sutter Biomedical, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1981

Total

Cleared

Denied

Sutter Biomedical, Inc. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 11 cleared submissions from 1981 to 1988. Primary specialty: Physical Medicine.

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

FDA 510(k) Regulatory Record - Sutter Biomedical, Inc.

11 devices

1-11 of 11

Cleared Feb 03, 1988

SUTTER PHALANGEAL CAP

K875249 · KWD

Orthopedic · 43d

Cleared Oct 09, 1987

SUTTER FINGER JOINT PROSTHESIS

K870200 · KYJ

Orthopedic · 262d

Cleared Sep 08, 1986

SUTTER LESSER METATARSAL CAP

K861983 · KWD

Orthopedic · 109d

Cleared Apr 25, 1985

SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT

K850274 · BXB

Physical Medicine · 92d

Cleared Apr 12, 1983

SUTTER CPM 5000

K830974 · JFA

Physical Medicine · 15d

Cleared Mar 17, 1983

SUTTER CPM 2000

K830649 · BXB

Physical Medicine · 16d

Cleared Jan 14, 1983

SUTTER CPM

K823539 · BXB

Physical Medicine · 45d

Cleared May 21, 1982

LESSER METATARSAL PHALANG. JOINT PROSTH

Physical Medicine · 16d

Cleared Nov 16, 1981

SILICONE IMPLANTS

K812691 · MDM

General & Plastic Surgery · 55d

Cleared Oct 14, 1981

PROXIMAL INTERPHALANGEAL JOINT IMPLANT

K802342 · JDI

Orthopedic · 383d

Sutter Biomedical, Inc. - FDA 510(k) Cleared Devices

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