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

DUET SUTURE ANCHOR

K Number: K020056 · Decision Jun 26, 2002
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
12
Review Days
169

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Basic Information

Device Name
DUET SUTURE ANCHOR
K Number
K020056
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bionx Implants, Ltd.
Date Received
January 8, 2002
Decision Date
June 26, 2002
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

Similar 510(k) Clearances

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

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Other Clearances by Bionx Implants, Ltd.

K Number Device Name
K030388 IMPACT SUTURE ANCHOR. MODEL 433510
K012001 SMARTSCREW
K012000 1.5MM BONE FIXATION KIT
K003077 SMARTSCREW MODEL 222006...227510
K003757 THERMOFX MESH
K000616 SMARTWEDGE ACL, MODELS 430623, 430628, 430723, 430728, 430823, 430828
K993074 SMART NAIL MODELS 521516, 521520,521525, 531516, 531520. 531525
K993073 SMART SCREW ACL MODELS 237020, 237025, 237030, 238020, 238025, 238030, 239020, 239025, 239030
K993453 MENISCUS ARROW, MODELS 531110, 531113, 531116
K992947 CANNULATED SMARTSCREW MODELS 224540C, 224570C
Search all 12 clearances from Bionx Implants, Ltd. →