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

BAR, DISTRACTION

K Number: K781841 · Decision Nov 8, 1978
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
84
Applicant Total
14
Review Days
12

Basic Information

Device Name
BAR, DISTRACTION
K Number
K781841
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
ACE ORTHOPEDIC MANUFACTURING CO.
Date Received
October 27, 1978
Decision Date
November 8, 1978
Product Code
JEC
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
JEC Component, Traction, Invasive

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