FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HOOK HOLLER

K Number: K770759 · Decision Apr 29, 1977
Classifications
1
FEI Numbers
115
Registration Numbers
115
Same Product Code
0
Applicant Total
303
Review Days
4

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Basic Information

Device Name
HOOK HOLLER
K Number
K770759
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Depuy, Inc.
Date Received
April 25, 1977
Decision Date
April 29, 1977
Product Code
KIK
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KIK Hook, Bone

Other Clearances by Depuy, Inc.

K Number Device Name
K043058 PINNACLE CONSTRAINED ACETABULAR LINERS
K042664 LPS UPPER EXTREMITY
K041085 LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARY
K033959 LPS
K040544 DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062
K021478 DELTA SHOULDER
K033329 DEPUY ACE UNIVERSAL AND TROCH ENTRY FEMORAL NAIL SYSTEMS
K032151 DEPUY SIGMA TIBIAL INSERTS AND CO-CR TIBIAL TRAYS
K020541 AGILITY ANKLE REVISION PROSTHESIS
K011810 ORTHOGENESIS LPS PROXIMAL TIBIAL REPLACEMENT AND ORTHOGENESIS LPS TIBIAL BEARING
Search all 303 clearances from Depuy, Inc. →