Atlas FDA

CERAMAX® Total Hip System

FDA premarket approval P070026/S084 · decided 2021-08-19

Approval details

PMA number
P070026
Supplement
S084
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
CERAMAX® Total Hip System
Generic name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
Applicant
DePuy Orthopaedics, Inc.
Date received
2021-07-21
Decision date
2021-08-19
Days to decision
29 days
Decision code
OK30
Product code
MRA
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
Manufacturing material change for the polishing process for the Ceramax Total Hip System.

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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