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

T.O.D. PLATE SYS STERILE

K Number: K842695 · Decision Sep 25, 1984
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
76
Review Days
76

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Basic Information

Device Name
T.O.D. PLATE SYS STERILE
K Number
K842695
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Kirschner Medical Corp.
Date Received
July 11, 1984
Decision Date
September 25, 1984
Product Code
KTT
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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Other Clearances by Kirschner Medical Corp.

K Number Device Name
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K942891 SUMMIT TOTAL HIP SYSTEM
K941486 INTEGRITY TOTAL HIP SYSTEM, NON-POROUS
K933843 LINE EXTENSION FOR KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM, POROUS COATED
K935951 KIRSCHNER C-2 OSTEOCAP TOTAL HIP SYSTEM
K935206 KIRSCHNER INTEGRITY ACETABULAR CUP MODIFICATION
K934589 KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM POROUS COATED
K934694 KIRSCHNER ZIRCONIA FEMORAL HEAD
K920188 THREADED PINS
Search all 76 clearances from Kirschner Medical Corp. →