Atlas FDA

FRACTURE/RECONSTRUCTION SYSTEM (TRAUMAONE)

FDA 510(k) clearance K081067 · decided 2008-05-09

Clearance details

K-number
K081067
Device name
FRACTURE/RECONSTRUCTION SYSTEM (TRAUMAONE)
Applicant
Biomet Microfixation, Inc.
Decision
Substantially Equivalent
Date received
2008-04-15
Decision date
2008-05-09
Days to decision
24 days
Clearance type
Special
Product code
JEY
Device class
2
Regulation number
872.4760
Medical specialty
Dental
Advisory committee
Dental
Location
Jacksonville, FL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Total Temporomandibular Joint Replacement System (P020016/S011)Biomet Microfixation, Inc.2019-12-17
TOTAL TEMPOROMANDIBULAR JOINT (TMJ) REPLACEMENT SYSTEM (P020016/S008)Biomet Microfixation, Inc.2017-06-08
TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM (P020016/S007)Biomet Microfixation, Inc.2014-12-09
TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM (P020016/S006)Biomet Microfixation, Inc.2012-03-15
TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM (P020016/S005)Biomet Microfixation, Inc.2010-11-08
TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM (P020016/S004)Biomet Microfixation, Inc.2010-01-29
TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM (P020016/S003)Biomet Microfixation, Inc.2009-10-21
TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM (P020016/S002)Biomet Microfixation, Inc.2006-10-13