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

MEMORY STAPLE (20 SIZES AVAILABLE)

K Number: K964226 · Decision Aug 5, 1997
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
15
Review Days
286

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Basic Information

Device Name
MEMORY STAPLE (20 SIZES AVAILABLE)
K Number
K964226
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Landos, Inc.
Date Received
October 23, 1996
Decision Date
August 5, 1997
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 Landos, Inc.

K Number Device Name
K971069 TWIST-OFF (TM) SCREW
K971070 SCARF THREAD-HEAD (TM) HEAD SCREW
K971068 34MM SCARF THREAD-HEAD(TM) SCREW
K961732 KAR
K970846 22.2/+4MM CO CR & ZIRCONIA FEMORAL HEAD
K953111 CORAIL
K962233 TWIST-OFF SCREW
K962236 SCARF THREAD-HEAD SCREW
K960642 NANCY NAIL
K943727 BIOSTOP G BONE CEMENT RESTRICTOR
Search all 15 clearances from Landos, Inc. →