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

HITCH LACTOSORB SUTURE ANCHOR

K Number: K061657 · Decision Jul 25, 2006
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
17
Review Days
42

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
HITCH LACTOSORB SUTURE ANCHOR
K Number
K061657
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrotek, Inc.
Date Received
June 13, 2006
Decision Date
July 25, 2006
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

Similar 510(k) Clearances

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

View all

Other Clearances by Arthrotek, Inc.

K Number Device Name
K061776 ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE
K061801 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS
K061389 ALLTHREAD LACTOSORB SUTURE ANCHOR
K060693 MICROSTRIKE AND ALLTHREAD PEEK 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. →