Atlas FDA

TRIATHLON TS KNEE SYSTEM

FDA 510(k) clearance K070095 · decided 2007-06-01

Clearance details

K-number
K070095
Device name
TRIATHLON TS KNEE SYSTEM
Applicant
Howmedica Osteonics Corp.
Decision
Substantially Equivalent
Date received
2007-01-10
Decision date
2007-06-01
Days to decision
142 days
Clearance type
Traditional
Product code
JWH
Device class
2
Regulation number
888.3560
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Mahwah, NJ, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp., A subsidiary recall (Z-1635-2015)Stryker Howmedica Osteonics Corp.2015-05-19
Stryker Orthopaedics Triathlon Femoral Distal Augment- Left; 1 single unit per package How recall (Z-1370-2013)Stryker Howmedica Osteonics Corp.2013-05-23
Triathlon Total Stabilizer Femoral Component; Size # 2 for Use with TS Components; Sterile recall (Z-0757-2010)Stryker Howmedica Osteonics Corp.2010-02-01
Triathlon Total Stabilizer Femoral Component; For Use with TS Components; Sterile, Made in recall (Z-0758-2010)Stryker Howmedica Osteonics Corp.2010-02-01
Triathlon Total Stabilizer Femoral Component; For Use with TS Components; Sterile, Made in recall (Z-0759-2010)Stryker Howmedica Osteonics Corp.2010-02-01
Triathlon Total Stabilizer Femoral Component; For Use with TS Components; Sterile, Made in recall (Z-0760-2010)Stryker Howmedica Osteonics Corp.2010-02-01
Triathlon Total Stabilizer Femoral Component; For Use with TS Components; Sterile, Made in recall (Z-0761-2010)Stryker Howmedica Osteonics Corp.2010-02-01
Offset Adaptor Trial - 2MM, Triathlon Revision Instruments. Non-Sterile; Howmedica Osteoni recall (Z-1607-2009)Stryker Howmedica Osteonics Corp.2009-07-23
Offset Adaptor Trial - 4MM, Triathlon Revision Instruments. Non-Sterile; Howmedica Osteoni recall (Z-1608-2009)Stryker Howmedica Osteonics Corp.2009-07-23
Offset Adaptor Trial - 6MM, Triathlon Revision Instruments. Non-Sterile; Howmedica Osteoni recall (Z-1609-2009)Stryker Howmedica Osteonics Corp.2009-07-23
Offset Adaptor Trial - 8MM, Triathlon Revision Instruments. Non-Sterile; Howmedica Osteoni recall (Z-1610-2009)Stryker Howmedica Osteonics Corp.2009-07-23
Triathlon-Press-Fit Stem These devices are modular components of a total knee system. Thes recall (Z-0890-2009)Stryker Howmedica Osteonics Corp.2009-01-26
Triathlon X3 Total Stabilizer + Tibial Insert For use with Triathlon Universal Baseplates, recall (Z-1231-2007)Stryker Howmedica Osteonics Corp.2007-09-25

PMA approvals by this applicant

RecordFirmDate
Trident Alumina Insert (625-0T-XXX); Osteonics® ABC/Trident® System (P000013/S027)Howmedica Osteonics Corp.2025-09-17
Trident Acetabular System: Trident Alumina Inserts (P000013/S026)Howmedica Osteonics Corp.2025-05-23
Trident® Acetabular System (P000013/S025)Howmedica Osteonics Corp.2024-03-08
Trident(R), ABC(R) (P000013/S024)Howmedica Osteonics Corp.2024-01-23
Trident Ceramic System (P000013/S021)Howmedica Osteonics Corp.2023-12-20
Trident(R), ABC(R) (P000013/S023)Howmedica Osteonics Corp.2023-12-19
Trident®, ABC® (P000013/S022)Howmedica Osteonics Corp.2023-09-27
Trident Acetabular System: Trident Alumina Inserts (P000013/S020)Howmedica Osteonics Corp.2022-04-01