Biomet, Inc. - FDA 510(k) Cleared Devices

Cleared Dec 21, 2004

MIMIX MP BONE VOID FILLER

K043280 · GXP

Neurology · 25d

Cleared Jul 08, 2004

ACUMEN SURGICAL NAVIGATION SYSTEM

K031454 · HAW

Neurology · 428d

Cleared Sep 22, 2003

ULTRA-DRIVE 3

K031280 · JDX

Neurology · 153d

Cleared Sep 15, 2003

ACUMEN SURGICAL NAVIGATION SYSTEM

K031337 · HAW

Neurology · 140d

Cleared May 05, 2003

BIOMET CRANIOFACIAL ACRYLIC CEMENT

K011399 · GXP

Neurology · 728d

Cleared Dec 21, 2001

MODIFICATION TO: INJECTABLE MIMIX

K012569 · GXP

Neurology · 134d

Cleared Nov 18, 1999

CRANIOFACIAL CALCIUM PHOSPHATE CERAMIC BONE FILLER

K990290 · GXP

Neurology · 293d

Cleared Feb 23, 1978

TRACTION UNITS

K780228 · HST

Neurology · 14d

Cleared Feb 23, 1978

TRACTION WEIGHT BAGS

K780233 · HST

Neurology · 14d