Atlas FDA

ABC TOTAL ELBOW PROTHESIS

FDA 510(k) clearance K972691 · decided 1997-10-15

Clearance details

K-number
K972691
Device name
ABC TOTAL ELBOW PROTHESIS
Applicant
Biomet, Inc.
Decision
Substantially Equivalent
Date received
1997-07-17
Decision date
1997-10-15
Days to decision
90 days
Clearance type
Traditional
Product code
JDB
Device class
2
Regulation number
888.3160
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Warsaw, IN, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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RHEAD RADIAL HEAD EXTENDED STEMS (K102180)Small Bone Innovations, Inc.2010-12-20
LATITUDE ELBOW PROSTHESIS (K100562)Tornier, Inc.2010-06-29
LATITUDE ELBOW PROTHESIS (K070787)Tornier2007-08-24
SBI LATERAL RADIO CAPITELLUM (K070236)Small Bone Innovations, Inc.2007-02-21
RHS (K060438)Tornier2006-04-18
SBI RADIO-CAPITELLAR IMPLANT (K060038)Small Bone Innovations, Inc.2006-03-30
TORNIER ELBOW PROSTHESIS (K050848)Tornier2005-07-14
MODIFICATION TO TORNIER TOTAL ELBOW PROSTHESIS (K031218)Tornier2003-05-16

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
C2A-TAPER ACETABULAR HIP SYSTEM (P050009/S009)Biomet, Inc.2011-02-11
C2A-TAPER ACETABULAR SYSTEM (P050009/S004)Biomet, Inc.2009-04-17
C2A TAPER ACETABULAR SYSTEM (P050009/S007)Biomet, Inc.2009-03-13
C2-A TAPER ACETABULAR SYSTEM (P050009/S005)Biomet, Inc.2007-11-30
C2A-TAPER ACETABULAR SYSTEM (P050009/S002)Biomet, Inc.2006-06-16
C2A-TAPER ACETABULAR SYSTEM (P050009/S001)Biomet, Inc.2006-02-01
C2 A-TAPER ACETABULAR SYSTEM (P050009)Biomet, Inc.2005-12-16