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

INSTRUMENT MAKAR PERFIX INTERFERENCE BONE SCREW

K Number: K930980 · Decision Feb 10, 1994
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
28
Review Days
350

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Basic Information

Device Name
INSTRUMENT MAKAR PERFIX INTERFERENCE BONE SCREW
K Number
K930980
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Instrument Makar, Inc.
Date Received
February 25, 1993
Decision Date
February 10, 1994
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

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Other Clearances by Instrument Makar, Inc.

K Number Device Name
K002600 LITWIN CRUICATE ANCHOR
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
K923841 BONE SCREWS
Search all 28 clearances from Instrument Makar, Inc. →