Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Screw, Fixation, Bone
510(k) Number K924018
Device Name M3 LAG SCREW FIXATION SYSTEM
Applicant
Osteomed Corp.
6062 San Fernando Rd.
Glendale,  CA  91202
Applicant Contact STEVEN C PUBOLS
Correspondent
Osteomed Corp.
6062 San Fernando Rd.
Glendale,  CA  91202
Correspondent Contact STEVEN C PUBOLS
Regulation Number888.3040
Classification Product Code
HWC  
Date Received08/11/1992
Decision Date 04/01/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-