Macropore Biosurgery, Inc. - FDA 510(k) Cleared Devices
17
Total
16
Cleared
0
Denied
Macropore Biosurgery, Inc. has 16 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 16 cleared submissions from 2000 to 2004.
Browse the FDA 510(k) cleared devices submitted by Macropore Biosurgery, Inc. Filter by specialty or product code using the sidebar.
17 devices
Cleared
Sep 20, 2004
MACROPORE PURICEL LIPOPLASTY SYSTEM
General & Plastic Surgery
28d
Cleared
Jul 28, 2004
MACROPORE HYDROSORB SPINE SYSTEM
Orthopedic
89d
Cleared
Sep 22, 2003
MACROPORE SURGI-WRAP MAST BIORESORBABLE SHEET
General & Plastic Surgery
89d
Cleared
Sep 04, 2003
MACROPORE CARDIO-WRAP (TS)
Cardiovascular
86d
Cleared
Jul 01, 2003
MACROPORE OS RECONSTRUCTION
General & Plastic Surgery
195d
Cleared
Feb 21, 2003
MACROPORE SURGICAL BARRIER FILM
Ophthalmic
114d
Cleared
Jul 01, 2002
MACROPORE OS TRAUMA
Orthopedic
81d
Cleared
Dec 03, 2001
MACROPORE SURGIWRAP (TS)
General & Plastic Surgery
158d
Cleared
Oct 25, 2001
MACROPORE ENT RECONSTRUCTION FILM
Ear, Nose, Throat
69d
Cleared
Sep 18, 2001
MACROPORE FX, PS, NS, LP
Dental
50d
Cleared
Aug 27, 2001
MACROPORE IB RESORBABLE PLUG
Orthopedic
84d
Cleared
Jul 20, 2001
MACROPORE OS SPINAL SYSTEM
Orthopedic
116d
Cleared
Jul 11, 2001
MACROPOREPX PEDIATRIC SYSTEM
Dental
355d
Cleared
May 02, 2001
MACROPORENS CRANILOC
Neurology
274d
Cleared
Oct 19, 2000
MACROPOREMX MANDIBULAR FIXATION SYSTEM
Dental
232d
Cleared
Jul 24, 2000
MACROSORBOS PROTECTIVE SHEET
Orthopedic
228d
Cleared
Jun 26, 2000
MACROPOREDX DISTRACTOR SYSTEM
Dental
90d