Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by ANDREW B ROGERS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190193
02/04/2019
SpineEX Sagittae« Lateral Lumbar Interbody Fusion Devices
SpineEX Inc.
K200816
03/30/2020
SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices
SpineEX, Inc.
K181531
06/11/2018
SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices
SpineEX Inc.
K223065
09/30/2022
Adcura« Sagittae« Lateral Lumbar Interbody Fusion Devices
Adcura, Inc.
K961120
03/21/1996
MARKER SYSTEM FOR STEREOTAXIC NAVIGATION
HOWMEDICA LEIBINGER, INC.
K961719
05/02/1996
EPITEC TITANIUM IMPLANT SYSTEM FOR THE SURGICAL ANCHORING OF FACIAL PROSTHESES
HOWMEDICA LEIBINGER, INC.
K963030
08/05/1996
LEIBINGER IMF SCREW
HOWMEDICA LEIBINGER, INC.
K954030
08/28/1995
BONE-LOCK
LEIBINGER GMBH
K963739
09/17/1996
LEIBINGER - LUHR SMALL ORTHOPEDIC BONE SCREWS
HOWMEDICA LEIBINGER, INC.
K963740
09/17/1996
LEIBINGER - LUHR SMALL MANDIBULAR BONE SCREWS
HOWMEDICA LEIBINGER, INC.
K963741
09/17/1996
LEIBINGER LUHR SMALL CRANIOMAXILLOFACIAL BONE SCREWS
HOWMEDICA LEIBINGER, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact