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510(k) K780891

Device
POST-OPERATIVE HIP ORTHOSIS
Applicant
HOSMER DORRANCE CORP.
510(k) number
K780891
Product code
ITS  
Decision
Substantially Equivalent (SESE)
Decision date
1978-06-13
Date received
1978-05-31
Regulation
890.3475
Classification name
Joint, Hip, External Brace
Medical specialty
Physical Medicine
Review panel
Physical Medicine
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Legacy Summary#

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FDA Review#

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