FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BIOKNOTLESS RC ANCHOR

K Number: K041064 · Decision May 13, 2004
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
13
Review Days
20

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Basic Information

Device Name
BIOKNOTLESS RC ANCHOR
K Number
K041064
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Depuy Mitek
Date Received
April 23, 2004
Decision Date
May 13, 2004
Product Code
JDR
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
JDR Staple, Fixation, Bone

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Other Clearances by Depuy Mitek

K Number Device Name
K243790 GRYPHON™ X Anchor; HEALIX TRANSTEND™ Anchor
K241010 HEALIX ADVANCE Knotless anchors; HEALIX ADVANCE Self-Punching anchors
K240441 MILAGRO Interference Screw; MILAGRO ADVANCE Interference Screw
K143475 VAPR Tripolar Suction Electrode
K120449 HEALIX ADVANCE PEEK ANCHOR
K080918 DOUBLE ARMED MENISCAL NEEDLES WITH SIZE #2-0 ORTHOCORD, MENISCAL NEEDLE WITH WIRE EYELET & 3 FREE STRANDS OF SIZE #2-0
K060664 FASTIN RC ANCHOR
K043298 BLUE ORTHOCORD SUTURE
K041117 PANALOK RC QUICKANCHOR PLUS, MODEL 212130, 212730; DUAL SUTURE PANALOK RC QUICKANCHOR PLLUS, MODELS 212132, 212732
K041116 SUPER QUICKANCHOR PLUS
Search all 13 clearances from Depuy Mitek →