SURGICAL SIMPLED P BONE CEMENT

FDA Premarket Approval N17003

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

DeviceSURGICAL SIMPLED P BONE CEMENT
Generic NameBone Cement
ApplicantHOWMEDICA CORP.
Date Received1971-10-07
Decision Date1971-10-07
PMAN17003
SupplementS
Product CodeLOD 
Advisory CommitteeOrthopedic
Expedited ReviewNo
Combination Product No
Applicant Address HOWMEDICA CORP. 359 Veterans Blvd. rutherford, NJ 07070

Supplemental Filings

Supplement NumberDateSupplement Type
N17003Original Filing
S004 1993-05-21 Normal 180 Day Track
S003 1991-10-08 Normal 180 Day Track
S002 1990-04-30 Normal 180 Day Track
S001 1981-03-03 Normal 180 Day Track

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.