FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

ACTIVATM PRODUCT GROUP INCLUDING BIOABSORBABLE DEVICES ACTIVAPIN FUSION, ACTIVANAILTM CONICALTM

K Number: K080879 · Decision Jun 24, 2008
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
200
Applicant Total
7
Review Days
85

Basic Information

Device Name
ACTIVATM PRODUCT GROUP INCLUDING BIOABSORBABLE DEVICES ACTIVAPIN FUSION, ACTIVANAILTM CONICALTM
K Number
K080879
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BIORETEC LTD
Date Received
March 31, 2008
Decision Date
June 24, 2008
Product Code
HTY
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
HTY Pin, Fixation, Smooth

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K071863 ACTIVAPIN, NEXFIX RFS PIN, NEXFIX RESORBABLE FIXATION SYSTEM (RFS)
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