Atlas FDA

Trident Ceramic System

FDA premarket approval P000013/S018 · decided 2021-03-05

Approval details

PMA number
P000013
Supplement
S018
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Trident Ceramic System
Generic name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
Applicant
Howmedica Osteonics Corp.
Date received
2021-01-05
Decision date
2021-03-05
Days to decision
59 days
Decision code
APPR
Product code
MRA
Advisory committee
Orthopedic
Expedited review
No
Location
Mahwah, NJ
Statement
Approval for a change in packaging of the Trident Alumina inserts which are part of the Trident Ceramic System. The foam raw material used to manufacture the foam packaging components will change from Opflex Microcell L1900/MC1900 to Vizion 2.0, and the foam packaging component tolerances listed on the foam packaging component drawings will be updated to +/- 0.120 inches to align the drawings with the manufacturing process currently used by the foam packaging component supplier.

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510(k) clearances by this applicant

RecordFirmDate
Exeter V40 Femoral Stem, Exeter X3 RimFit Cup (K193429)Howmedica Osteonics Corp.2020-08-13
Triathlon Posterior Stabilized Femoral Component - beaded with Peri-Apatite, Triathlon Cruciate Retaining Femoral Component - beaded with Peri-Apatite (K200782)Howmedica Osteonics Corp.2020-05-13
REUNION RSA SHOULDER SYSTEM (K130895)Howmedica Osteonics Corp.2013-12-27
ABG III MONOLITHIC HIP STEM (K123604)Howmedica Osteonics Corp.2013-08-16
DISTAL FEMORAL GROWING PROSTHESIS, TIBIAL ROTATING COMPONENTS, BEARING, AXIS, CIRCLIP, WEDGE (K122015)Howmedica Osteonics Corp.2013-02-22
TRIATHLON ALL-POLYETHYLENE CONDYLAR STABILIZING (CS) TIBIAL IMPLANTS TRIATHLON ALL-POLYETHYLENE POSTERIOR STABILIZING (P (K123166)Howmedica Osteonics Corp.2013-02-14
NOVEL FIT AND FILL STEM (K122853)Howmedica Osteonics Corp.2013-02-01
STRYKER CMF MEDPOR CUSTOMIZED IMPLANT (K121315)Howmedica Osteonics Corp.2012-11-01