Atlas FDA

ORTHOLOGIC 1000 BONE GROWTH STIMULATOR/PATIENT REGISTRY MARKETING BROCHURE

FDA premarket approval P910066/S013 · decided 1999-04-20

Approval details

PMA number
P910066
Supplement
S013
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
ORTHOLOGIC 1000 BONE GROWTH STIMULATOR/PATIENT REGISTRY MARKETING BROCHURE
Generic name
Stimulator, bone growth, non-invasive
Applicant
Djo, LLC
Date received
1999-02-22
Decision date
1999-04-20
Days to decision
57 days
Decision code
APPR
Product code
LOF
Advisory committee
Orthopedic
Expedited review
No
Location
Vista, CA
Statement
Approval for updating the Patient Registry Data Sheet.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
Compex Sport Elite 3.0 (K201653)Djo, LLC2020-11-27
Compex Sport Elite (K170918)Djo, LLC2017-06-20
Compex Wireless USA (K170903)Djo, LLC2017-06-19
Strive (K153704)Djo, LLC2016-06-03
Chattanooga Revolution Wireless (K153696)Djo, LLC2016-04-14
VitalStim(R) Plus Electrotherapy System (K153224)Djo, LLC2016-02-17
Compex Wireless USA (K143551)Djo, LLC2015-04-28
VECTRA NEO CLINICAL THERAPY SYSTEM (K132284)Djo, LLC2014-04-10