FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

COVENTRY STAPLE

K Number: K761064 · Decision Dec 30, 1976
Classifications
1
FEI Numbers
168
Registration Numbers
168
Same Product Code
279
Applicant Total
303
Review Days
42

Basic Information

Device Name
COVENTRY STAPLE
K Number
K761064
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4750
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
DEPUY, INC.
Date Received
November 18, 1976
Decision Date
December 30, 1976
Product Code
GDW
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
GDW Staple, Implantable

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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
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