Elite Surgical Supplies (Pty), Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Elite Surgical Supplies (Pty), Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Biolign® Roto-Loc Cervical Plate System
4
Total
4
Cleared
0
Denied
Elite Surgical Supplies (Pty), Ltd. has 4 FDA 510(k) cleared medical devices. Based in Marietta, US.
Historical record: 4 cleared submissions from 2007 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Elite Surgical Supplies (Pty), Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jalex Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Elite Surgical Supplies (Pty), Ltd.
4 devices
Cleared
Apr 30, 2020
Biolign® Roto-Loc Cervical Plate System
Orthopedic
59d
Cleared
Oct 29, 2013
BIOLIGN ACIF SYSTEMS, BIOLIGN STACC ACIF SYSTEM, BIOLIGN TLIF SYSTEM
Orthopedic
267d
Cleared
Jan 28, 2008
MODIFICATION TO: VERTEFIX PEDICLE SCREW SPINAL SYSTEM
Orthopedic
17d
Cleared
Aug 30, 2007
VERTEFIX PEDICLE SCREW SPINAL SYSTEM
Orthopedic
288d