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

1-CUT ACL GRAFT KNIFE

K Number: K905380 · Decision Dec 13, 1990
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
25
Applicant Total
303
Review Days
13

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Basic Information

Device Name
1-CUT ACL GRAFT KNIFE
K Number
K905380
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
November 30, 1990
Decision Date
December 13, 1990
Product Code
GDX
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
GDX Scalpel, One-Piece

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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
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