Atlas FDA

ATTUNE Revision RP Tibial Base

FDA premarket approval P830055/S204 · decided 2018-06-25

Approval details

PMA number
P830055
Supplement
S204
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ATTUNE Revision RP Tibial Base
Generic name
Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing
Applicant
Depuy, Inc.
Date received
2018-06-04
Decision date
2018-06-25
Days to decision
21 days
Decision code
OK30
Product code
NJL
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
Modification to the Blast Plug used in the manufacturing process for the ATTUNE Revision RP Tibial Base.

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510(k) clearances by this applicant

RecordFirmDate
PINNACLE CONSTRAINED ACETABULAR LINERS (K043058)Depuy, Inc.2005-03-14
LPS UPPER EXTREMITY (K042664)Depuy, Inc.2004-12-08
LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARY (K041085)Depuy, Inc.2004-07-22
LPS (K033959)Depuy, Inc.2004-07-01
DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062 (K040544)Depuy, Inc.2004-05-28
DELTA SHOULDER (K021478)Depuy, Inc.2003-11-18
DEPUY ACE UNIVERSAL AND TROCH ENTRY FEMORAL NAIL SYSTEMS (K033329)Depuy, Inc.2003-11-14
DEPUY SIGMA TIBIAL INSERTS AND CO-CR TIBIAL TRAYS (K032151)Depuy, Inc.2003-09-26