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

MENISCUS ARROW SHEATH #CN1000A; SMARTSCREW ACL SHEATH #SSA2000A

K Number: K010554 · Decision May 25, 2001
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
18
Review Days
88

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Basic Information

Device Name
MENISCUS ARROW SHEATH #CN1000A; SMARTSCREW ACL SHEATH #SSA2000A
K Number
K010554
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, Inc.
Date Received
February 26, 2001
Decision Date
May 25, 2001
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, Inc.

K Number Device Name
K023022 NUGEN FX SCREW
K011569 BIOSORBFX O/M 2.0/2/4 SYSTEM
K013546 MODIFICATION TO: 1.5 BONE FIXATION KIT, MODELS BXS6114, BXS6214
K013057 BIOCUFF,C, MODELS 236018, 236028, 236036
K012334 CONTOUR MENISCUS ARROW, MODELS 541110, 541113, AND 541116
K010983 PLLA PIN
K010687 BIOSORBFX AND BIOSORBPDX MESH
K003659 PLGA PIN, MODEL 171120,171140,171520,171540,171560,172020,172040,172060,173240,173260
K003970 CONTOUR LABRAL NAIL, MODEL 533520A
K003756 BIOSORBFX TACK AND BIOSORBPDX TACK BIOABSORBABLE FIXATION FASTENER, USED WITH PLATES
Search all 18 clearances from Bionx Implants, Inc. →