Hall Surgical, Division of Zimmer, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Hall Surgical, Division of Zimmer, Inc. has 8 FDA 510(k) cleared medical devices. Based in `Anta Barbara, US.
Historical record: 8 cleared submissions from 1985 to 1994. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Hall Surgical, Division of Zimmer, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Hall Surgical, Division of Zimmer, Inc.
8 devices
Cleared
Sep 07, 1994
HALL MICROCHOICE ELECTRIC POWERED SYSTEM
Orthopedic
93d
Cleared
Feb 10, 1987
HALL ORAL IMPLANT SYSTEM
Dental
68d
Cleared
Jan 28, 1987
HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYST
Orthopedic
43d
Cleared
Nov 20, 1986
HALL DUNBAR DRILL GUIDE SYSTEM
Orthopedic
28d
Cleared
Sep 08, 1986
HALL CANNLULA SYSTEM
Orthopedic
48d
Cleared
Jul 17, 1986
HALL STERNUM SAW
General & Plastic Surgery
17d
Cleared
Jul 15, 1986
HALL STERILE BUR
Orthopedic
13d
Cleared
Jun 26, 1985
HALL IRRIGATION SYSTEM
General & Plastic Surgery
41d