V. Mueller Neuro/Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
V. Mueller Neuro/Spine - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
V. Mueller Neuro/Spine has 8 FDA 510(k) cleared medical devices. Based in San Carlos, US.
Historical record: 8 cleared submissions from 1994 to 2000. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by V. Mueller Neuro/Spine Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - V. Mueller Neuro/Spine
8 devices
Cleared
Aug 29, 2000
PSI SKULL CLAMP
Neurology
34d
Cleared
Mar 30, 2000
PACIFIC SURGICAL PATTIES
Neurology
204d
Cleared
Jan 06, 2000
PSI TITANIUM ANEURYSM CLIP
Neurology
210d
Cleared
Jun 11, 1999
PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIP
General & Plastic Surgery
78d
Cleared
Jul 09, 1998
TAKA ANEURYSM CLIP
Neurology
351d
Cleared
Jan 23, 1997
VERSATRAC (TM) LUMBAR RETRACTOR SYSTEM
Neurology
80d
Cleared
Dec 27, 1994
PSI FLEXIBLE ARM
General & Plastic Surgery
209d
Cleared
Dec 07, 1994
ULTRA-LINE RONGEUR
Neurology
133d