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

LARGE UNI-CLIP STAPLE

K Number: K061594 · Decision Jul 3, 2006
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
28
Review Days
25

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Basic Information

Device Name
LARGE UNI-CLIP STAPLE
K Number
K061594
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
New Deal, S.A.
Date Received
June 8, 2006
Decision Date
July 3, 2006
Product Code
JDR
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
JDR Staple, Fixation, Bone

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K061765 KALIX II IMPLANT
K060476 LAPIDUS PLATE
K060473 TTC PLATE
K053093 KALIX II IMPLANT, MODEL 141 0XX WITH XX
K052152 B-BOP PLATE
K050882 NEWDEAL ANKLE NAIL
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