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

COLBALT ALLOY ORTHOPAEDIC WIRE

K Number: K811500 · Decision Jun 18, 1981
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
178
Review Days
22

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Basic Information

Device Name
COLBALT ALLOY ORTHOPAEDIC WIRE
K Number
K811500
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Osteonics Corp.
Date Received
May 27, 1981
Decision Date
June 18, 1981
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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