Medical Device Manufacturer · US , Fall River , MA

Pfizer Hospital Products Group, Inc. - FDA 510(k) Cleared Devices

8 submissions · 7 cleared · Since 1991

8

Total

7

Cleared

0

Denied

Pfizer Hospital Products Group, Inc. has 7 FDA 510(k) cleared medical devices. Based in Fall River, US.

Historical record: 7 cleared submissions from 1991 to 1994. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Pfizer Hospital Products Group, Inc.

8 devices

1-8 of 8

Cleared Feb 22, 1994

MEGA PLUS SUPER LAG SCREW

Orthopedic · 405d

Cleared Aug 18, 1992

DURACON TOTAL KNEE SYSTEM TIBIAL COMPONENTS

Orthopedic · 253d

Cleared Jun 10, 1992

PCA TOTAL HIP SYSTEM (CEMENTLESS USE)

Orthopedic · 111d

Cleared Mar 18, 1992

DURACON MODULAR FEMORAL COMPONENT AND FEMORAL SPAC

Orthopedic · 72d

Cleared Jan 31, 1992

HOWMEDICA ALUMINA FEMORAL HEAD

Orthopedic · 74d

Cleared Aug 13, 1991

PLEUR-EVAC PLUS CONTIN. REINFUS. & AUTOINFUS. SYST

Anesthesiology · 123d

Cleared May 01, 1991

SCHNEIDER WALLSTENT(R)

Gastroenterology & Urology · 37d

Cleared Mar 14, 1991

BONDEK POLYGLYCOLIC ACID SYNTHETIC ABSORB. SUTURE

General & Plastic Surgery · 98d