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

ACTIVAPIN

K Number: K061164 · Decision Jul 6, 2006
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
9
Review Days
71

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Basic Information

Device Name
ACTIVAPIN
K Number
K061164
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
April 26, 2006
Decision Date
July 6, 2006
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HTY), ordered by most recent decision date.

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Other Clearances by Bioretec, Ltd.

K Number Device Name
DEN220030 RemeOs™ Screw LAG Solid
K133950 ACTIVAPIN HT, FUSE LINK (PRIVATE LABLED FOR FOOTMIND, INC.)
K130716 BIORETEC ACTIVASCREW INTERFERENCE
K080879 ACTIVATM PRODUCT GROUP INCLUDING BIOABSORBABLE DEVICES ACTIVAPIN FUSION, ACTIVANAILTM CONICALTM
K081392 BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN
K072848 ACTIVASCREW
K071863 ACTIVAPIN, NEXFIX RFS PIN, NEXFIX RESORBABLE FIXATION SYSTEM (RFS)
K062980 ACTIVASCREW