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

LITWIN CRUICATE ANCHOR

K Number: K002600 · Decision Nov 15, 2000
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
28
Review Days
86

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Basic Information

Device Name
LITWIN CRUICATE ANCHOR
K Number
K002600
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Instrument Makar, Inc.
Date Received
August 21, 2000
Decision Date
November 15, 2000
Product Code
MBI
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
MBI Fastener, Fixation, Nondegradable, Soft Tissue

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Other Clearances by Instrument Makar, Inc.

K Number Device Name
K980999 ST LEGER CEMENTED SEMI-CONSTRAINED TOTAL KNEE IMPLANT
K963396 BIOSPHERE SUTURE ANCHOR
K964364 DISPOSABLE APRON
K955835 FLUID BARRIER BOOT KNEE & ANKLE-HIGH
K960555 BIOASBSORBABLE MINI-SCREW SUTURE ANCHOR
K943249 BIOABSORBABLE INTERFERENCE SCREW
K942828 MAKAR FULL AND HALF FACE SHIELD
K944062 LAPRASCOPIC GRASPER
K930980 INSTRUMENT MAKAR PERFIX INTERFERENCE BONE SCREW
K923841 BONE SCREWS
Search all 28 clearances from Instrument Makar, Inc. →