Atlas FDA

DEPUY CERAMAX TOTAL HIP SYSTEM

FDA premarket approval P070026/S012 · decided 2013-08-06

Approval details

PMA number
P070026
Supplement
S012
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
DEPUY CERAMAX TOTAL HIP SYSTEM
Generic name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
Applicant
DePuy Orthopaedics, Inc.
Date received
2013-03-12
Decision date
2013-08-06
Days to decision
147 days
Decision code
APPR
Product code
MRA
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
APPROVAL FOR CHANGES TO THE PROCESS PARAMETERS FOR AN EXISTING PACKAGE SEALER AND ADDITION OF AN ALTERNATE PACKAGE SEALER.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
DePuy ATTUNE™ Knee System (K252887)DePuy Orthopaedics, Inc.2026-05-22
CUPTIMIZE™ Advanced (K231503)DePuy Orthopaedics, Inc.2023-08-22
DePuy Corail AMT Hip Prosthesis (K213839)DePuy Orthopaedics, Inc.2022-01-06
DELTA XTEND Reverse Shoulder System (K210167)DePuy Orthopaedics, Inc.2021-02-19
DePuy Corail AMT Hip Prosthesis (K203167)DePuy Orthopaedics, Inc.2020-11-19
ACTIS Duofix Hip Prosthesis (K202472)DePuy Orthopaedics, Inc.2020-10-21
DePuy ATTUNE™ Total Knee System (K201347)DePuy Orthopaedics, Inc.2020-06-18
TRUMATCH Personalized Solutions (K193540)DePuy Orthopaedics, Inc.2020-06-16