510(k) K770759

Device: HOOK HOLLER
Applicant: Depuy, Inc.
510(k) number: K770759
Product code: KIK
Decision: Substantially Equivalent (SESE)
Decision date: 1977-04-29
Date received: 1977-04-25
Regulation: 878.4800
Classification name: Hook, Bone
Medical specialty: General, Plastic Surgery
Review panel: General, Plastic Surgery
Device class: 1
Clearance type: Traditional
Third party reviewed: N

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