Mcconnell Orthopedic is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mcconnell Orthopedic - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Mcconnell Orthopedic has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Dallas, US.
Historical record: 16 cleared submissions from 1987 to 1991.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mcconnell Orthopedic
16 devices
Cleared
Mar 21, 1991
MCCONNELL SHOULDER BRACE
Physical Medicine
14d
Cleared
Feb 21, 1991
PREP AND OPERATING STAND
General & Plastic Surgery
71d
Cleared
Feb 21, 1991
LATERAL BUTTRESS SUPPORT
General & Plastic Surgery
71d
Cleared
Jan 13, 1989
MCCONNELL REAMER GUIDE
Orthopedic
32d
Cleared
May 26, 1987
MCCONNELL ORTHOPEDIC ANTERIOR TORSO-ARM SUPPORT
General & Plastic Surgery
15d
Cleared
May 26, 1987
MCCONNELL ORTHOPEDIC POSTERIOR BODY SUPPORT
General & Plastic Surgery
15d
Cleared
May 26, 1987
MCCONNELL ORTHOPEDIC U-HOOK ASSEMBLY
General & Plastic Surgery
15d
Cleared
May 26, 1987
MCCONNELL ORTHOPEDIC TIBIAL POSITIONER
General & Plastic Surgery
15d
Cleared
May 26, 1987
MCCONNELL ORTHOPEDIC SUSPENSION SYSTEM
General & Plastic Surgery
15d
Cleared
May 26, 1987
MCCONNELL ORTHOPEDIC PELVIC CALIPER SUPPORT
General & Plastic Surgery
14d
Cleared
May 26, 1987
MCCONNELL ORTHOPEDIC ANKLE POSITIONER
General & Plastic Surgery
14d
Cleared
May 22, 1987
MCCONNELL ORTHOPEDIC SHOULDER/HIP POSITIONER
General & Plastic Surgery
11d