Atlas FDA

TORNIER ELBOW PROSTHESIS

FDA 510(k) clearance K050848 · decided 2005-07-14

Clearance details

K-number
K050848
Device name
TORNIER ELBOW PROSTHESIS
Applicant
Tornier
Decision
Substantially Equivalent
Date received
2005-04-04
Decision date
2005-07-14
Days to decision
101 days
Clearance type
Traditional
Product code
JDB
Device class
2
Regulation number
888.3160
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Monbonnot Saint Martin, FR
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
TEMA Elbow system - Line extension (K222807)Lima Corporate S.P.A.2022-10-26
LATITUDE EV™ Total Elbow Arthroplasty (K193247)Tornier, Inc.2020-08-05
LATITUDE EV Total Elbow Arthroplasty (K182461)Tornier, Inc.2018-12-27
Latitude EV Total Elbow Arthroplasty (K171010)Tornier, Inc.2017-08-31
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
MODIFICATION TO TORNIER TOTAL ELBOW PROSTHESIS (K031218)Tornier2003-05-16
TORNIER TOTAL ELBOW PROSTHESIS (K011567)Tornier2001-06-19

Recalls involving this device

No recalls on record reference this clearance.