Macropore Biosurgery, Inc.
Macropore Biosurgery, Inc. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2004.
Top product codes for Macropore Biosurgery, Inc.
Recent clearances by Macropore Biosurgery, Inc.
- K042261 — MACROPORE PURICEL LIPOPLASTY SYSTEM
- K041105 — MACROPORE HYDROSORB SPINE SYSTEM
- K031955 — MACROPORE SURGI-WRAP MAST BIORESORBABLE SHEET
- K031785 — MACROPORE CARDIO-WRAP (TS)
- K024169 — MACROPORE OS RECONSTRUCTION
- K023643 — MACROPORE SURGICAL BARRIER FILM
- K021164 — MACROPORE OS TRAUMA
- K012025 — MACROPORE SURGIWRAP (TS)
- K012769 — MACROPORE ENT RECONSTRUCTION FILM
- K012413 — MACROPORE FX, PS, NS, LP
- K011715 — MACROPORE IB RESORBABLE PLUG
- K010911 — MACROPORE OS SPINAL SYSTEM
- K002207 — MACROPOREPX PEDIATRIC SYSTEM
- K002334 — MACROPORENS CRANILOC
- K000696 — MACROPOREMX MANDIBULAR FIXATION SYSTEM
- K994158 — MACROSORBOS PROTECTIVE SHEET
- K000992 — MACROPOREDX DISTRACTOR SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.