Medical Device Manufacturer · US , North Oaks , MN

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

17 submissions · 17 cleared · Since 1985

Total

Cleared

Denied

Cedar Surgical, Inc. has 17 FDA 510(k) cleared medical devices. Based in North Oaks, US.

Historical record: 17 cleared submissions from 1985 to 1987. Primary specialty: General & Plastic Surgery.

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

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

17 devices

1-12 of 17

Cleared Dec 17, 1987

RAYLOR(TM) DRILL STOP

General & Plastic Surgery · 139d

Cleared Oct 26, 1987

CEDAR(TM) PELVIC CUSHION

K873690 · LWG

General & Plastic Surgery · 48d

Cleared Sep 28, 1987

CEDAR(TM) RETRACTOR RING

K873691 · GZT

Neurology · 20d

Cleared Dec 12, 1986

RAYLOR(TM) DISSECTING HOOK

K864425 · GDG

General & Plastic Surgery · 32d

Cleared Nov 26, 1986

RAYLOR(TM) PERIOSTEAL ELEVATORS

K864421 · GEG

General & Plastic Surgery · 16d

Cleared Nov 26, 1986

RAYLOR(TM) PROTECTIVE RETRACTOR

K864424 · GAD

General & Plastic Surgery · 16d

Cleared Nov 26, 1986

RAYLOR(TM) DEPTH GAUGE

RAYLOR(TM) OSTEOTOMES

K864423

Orthopedic · 14d

Cleared Sep 24, 1986

RAYLOR BONE IMPACTORS

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

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