Medical Device Manufacturer · US , Walker , MI

Plastafil, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1984

Total

Cleared

Denied

Plastafil, Inc. has 13 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 13 cleared submissions from 1984 to 1984. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Plastafil, Inc.

13 devices

1-12 of 13

General & Plastic Surgery · 130d

Cleared Aug 27, 1984

THREADING TUBE

K841618 · FZX

General & Plastic Surgery · 130d

General & Plastic Surgery · 130d

General & Plastic Surgery · 83d

Cleared Jul 11, 1984

SOFT-TISSUE INSTRUMENT

K841622 · HWQ

Orthopedic · 83d

Plastafil, Inc. - FDA 510(k) Cleared Devices

Filters