510(k) K802348

Device
TRIAXIAL
Applicant
JOHNSON & JOHNSON PROFESSIONALS, INC.
510(k) number
K802348
Product code
JDB  
Decision
Substantially Equivalent (SESE)
Decision date
1981-02-23
Date received
1980-09-25
Regulation
888.3160
Classification name
Prosthesis, Elbow, Semi-constrained, Cemented
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
325 Paramount Dr. Raynham MA US 02767 02767

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JDB  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K222807TEMA Elbow system - Line extensionLima Corporate S.P.A.2022-10-26
K193247LATITUDE EV™ Total Elbow ArthroplastyTornier, Inc.2020-08-05
K182461LATITUDE EV Total Elbow ArthroplastyTornier, Inc.2018-12-27
K171010Latitude EV Total Elbow ArthroplastyTornier, Inc.2017-08-31
K102180RHEAD RADIAL HEAD EXTENDED STEMSSmall Bone Innovations, Inc.2010-12-20
K100562LATITUDE ELBOW PROSTHESISTornier, Inc.2010-06-29
K070787LATITUDE ELBOW PROTHESISTornier2007-08-24
K070236SBI LATERAL RADIO CAPITELLUMSmall Bone Innovations, Inc.2007-02-21
K060438RHSTornier2006-04-18
K060038SBI RADIO-CAPITELLAR IMPLANTSmall Bone Innovations, Inc.2006-03-30
K050848TORNIER ELBOW PROSTHESISTornier2005-07-14
K031218MODIFICATION TO TORNIER TOTAL ELBOW PROSTHESISTornier2003-05-16
K011567TORNIER TOTAL ELBOW PROSTHESISTornier2001-06-19
K983141CAPITELLO-CONDYLAR TOTAL ELBOW PROSTHESISJohnson & Johnson Professionals, Inc.1998-11-06
K972691ABC TOTAL ELBOW PROTHESISBiomet, Inc.1997-10-15

Legacy Summary#

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FDA Review#

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