← DeviceClear
HomeDevice Clearances

CRANIOFACIAL ANCHORS — Biomet, Inc. (510(k) K974136)

CRANIOFACIAL ANCHORS — Biomet, Inc. (510(k) K974136) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: CRANIOFACIAL ANCHORS; Applicant: Biomet, Inc.; Clearance track: 510(k).

Device nameCRANIOFACIAL ANCHORS
ApplicantBiomet, Inc.
Clearance track510(k)
Submission numberK974136
DecisionSubstantially Equivalent
Decision date1998-01-30
Date received1997-11-03
Product codeMBI
Device class2
Medical specialtyOrthopedic
Applicant locationIN, US
SourceopenFDA device

🔍 Search all device clearances →