Atlas FDA

LITHOTRON ULS

FDA premarket approval P970019/S006 · decided 1999-12-17

Approval details

PMA number
P970019
Supplement
S006
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
LITHOTRON ULS
Generic name
Lithotriptor, extracorporeal shock-wave, urological
Applicant
Healthtronics Surgical Services, Inc.
Date received
1999-07-06
Decision date
1999-12-17
Days to decision
164 days
Decision code
APRL
Product code
LNS
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Marietta, GA
Statement
Approval for addition of an ultrasonic stone location accessory. The device is indicated for preliminary localization of a target stone prior to extracorporeal shock wave lithotripsy with the Lithotron(TM) Lithotripsy System. The indications for use have not changed.

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510(k) clearances by this applicant

RecordFirmDate
TWINTRODE ELC 134 ELECTRODE (K012785)Healthtronics Surgical Services, Inc.2001-11-16
HEALTHTRONIC OMEGA TRAC (K881902)Healthtronics Surgical Services, Inc.1988-06-22