FDA Device Intelligence
HomeMEDTRONIC POWERED SURGICAL SOLUTIONS › MIDAS REX BONE MILL

MIDAS REX BONE MILL

MEDTRONIC POWERED SURGICAL SOLUTIONS · Model BM120 · UDI-DI 00763000293758

LYSHBC Prescription
4
510(k) clearances
1,273
Adverse events
1
Recalls
85
Facilities

Description

CONSOLE BM120 ELECTRIC BONE MILL ROHS

Recalls

DateFirmReason
2006-10-20Medtronic Sofamor Danek USA IncMetal bone fragmentor was causing metal shavings to be released into the resultant fragmented tissue during use.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.