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

BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN

K Number: K081392 · Decision Jun 18, 2008
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
9
Review Days
30

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Basic Information

Device Name
BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN
K Number
K081392
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bioretec, Ltd.
Date Received
May 19, 2008
Decision Date
June 18, 2008
Product Code
HWC
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
HWC Screw, Fixation, Bone

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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
K072848 ACTIVASCREW
K071863 ACTIVAPIN, NEXFIX RFS PIN, NEXFIX RESORBABLE FIXATION SYSTEM (RFS)
K062980 ACTIVASCREW
K061164 ACTIVAPIN