Arthropedics, Inc. - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Arthropedics, Inc. has 29 FDA 510(k) cleared medical devices. Based in Wallington, US.
Historical record: 29 cleared submissions from 1987 to 1988. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Arthropedics, Inc. Filter by specialty or product code using the sidebar.
29 devices
Cleared
Jan 14, 1988
ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)
Orthopedic
128d
Cleared
Dec 15, 1987
MONOPOLAR CAUTERY BLADE TIP #TM-1701
General & Plastic Surgery
96d
Cleared
Dec 15, 1987
MONOPOLAR CAUTERY CONICAL TIP #TM-1702
General & Plastic Surgery
96d
Cleared
Dec 15, 1987
MONOPOLAR CAUTERY RETROGADE TIP #TM-1703
General & Plastic Surgery
96d
Cleared
Nov 25, 1987
VIDEO ARTHROSCOPE, 1.7MM X 55 MM
General & Plastic Surgery
152d
Cleared
Nov 02, 1987
THE CART
Orthopedic
129d
Cleared
Nov 02, 1987
SCISSOR, LEFT
Orthopedic
63d
Cleared
Nov 02, 1987
SCISSOR, RIGHT
Orthopedic
63d
Cleared
Nov 02, 1987
CUP BIOPSY FORCEPS, LEFT
General & Plastic Surgery
63d
Cleared
Nov 02, 1987
CUP BIOPSY FORCEPS, RIGHT
General & Plastic Surgery
63d
Cleared
Nov 02, 1987
CUP BIOPSY FORCEPS, CURVED DOWN
General & Plastic Surgery
63d
Cleared
Nov 02, 1987
CUP BIOPSY FORCEPS, CURVED UP
General & Plastic Surgery
63d