STORZ MODULITH LITHOTRIPTER, MODEL SLX

FDA Premarket Approval P920051 S005

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Approval for changes to the x-ray imaging system of the storz modulith(r) lithotripter, model slx.

DeviceSTORZ MODULITH LITHOTRIPTER, MODEL SLX
Generic NameLithotriptor, Extracorporeal Shock-wave, Urological
ApplicantKARL STORZ ENDOSCOPY-AMERICA, INC.
Date Received1996-10-08
Decision Date1996-12-27
PMAP920051
SupplementS005
Product CodeLNS 
Advisory CommitteeGastroenterology/Urology
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address KARL STORZ ENDOSCOPY-AMERICA, INC. 1201 Roberts Blvd. kennesaw, GA 30144

Supplemental Filings

Supplement NumberDateSupplement Type
P920051Original Filing
S007 1997-10-02 Special (immediate Track)
S006 1997-03-26 Real-time Process
S005 1996-10-08 Normal 180 Day Track
S004 1996-08-30 Normal 180 Day Track
S003 1996-04-17 Normal 180 Day Track
S002 1995-09-18 Normal 180 Day Track
S001 1995-07-24 Normal 180 Day Track

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