S-ROM POLY-DIAL CONSTRAINED LINER

FDA Premarket Approval P960054

This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.

Pre-market Approval Supplement Details

Approval for the johnson and johnson's s-rom poly-dial constrained acetabular liner. This device is indicated for use as a component of a total hip prosthesis in primary or revision patients at high risk of hip dislocation due to a history of prior dislocation, bone loss, joint or soft tissue laxity, neuromuscular disease or intraoperative instability.

DeviceS-ROM POLY-DIAL CONSTRAINED LINER
Generic NameProsthesis, Hip, Constrained, Cemented Or Uncemented, Metal/polymer
ApplicantDEPUY, A JOHNSON & JOHNSON CO.
Date Received1996-12-26
Decision Date1997-06-19
Notice Date1997-10-07
PMAP960054
SupplementS
Product CodeKWZ 
Docket Number97M-0416
Advisory CommitteeOrthopedic
Expedited ReviewNo
Combination Product No
Applicant Address DEPUY, A JOHNSON & JOHNSON CO. p.o. Box 988 700 Orthopaedic Drive warsaw, IN 46581-0988

Supplemental Filings

Supplement NumberDateSupplement Type
P960054Original Filing
S004 1999-10-06 Normal 180 Day Track
S003 1999-08-10 Normal 180 Day Track
S002 1999-07-30 Normal 180 Day Track
S001

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