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

MODIFICATION TO THE TAC' PIN

K Number: K011875 · Decision Sep 6, 2001
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
93
Applicant Total
28
Review Days
83

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Basic Information

Device Name
MODIFICATION TO THE TAC' PIN
K Number
K011875
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
New Deal, S.A.
Date Received
June 15, 2001
Decision Date
September 6, 2001
Product Code
JDW
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
JDW Pin, Fixation, Threaded

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K Number Device Name
K070241 MODIFICATION TO LAPIDUS PLATE
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K063820 LISFRANC PLATE
K060474 LISFRANC PLATE
K061765 KALIX II IMPLANT
K061594 LARGE UNI-CLIP STAPLE
K060476 LAPIDUS PLATE
K060473 TTC PLATE
K053093 KALIX II IMPLANT, MODEL 141 0XX WITH XX
K052152 B-BOP PLATE
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