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

MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR

K Number: K060693 · Decision Jun 6, 2006
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
17
Review Days
83

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Basic Information

Device Name
MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR
K Number
K060693
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrotek, Inc.
Date Received
March 15, 2006
Decision Date
June 6, 2006
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 Arthrotek, Inc.

K Number Device Name
K061776 ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE
K061801 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS
K061657 HITCH LACTOSORB SUTURE ANCHOR
K061389 ALLTHREAD LACTOSORB SUTURE ANCHOR
K053461 EZLOC FEMORAL FIXATION DEVICE
K051069 NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHER
K042460 TI - SCREW ANCHOR SP
K041274 RESORBABLE INTERFERENCE SCREW
K041261 FEMORAL HOOK
K040604 INNERVUE DIAGNOSTIC SCOPE SYSTEM
Search all 17 clearances from Arthrotek, Inc. →