FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

GOLDEN RETRIEVERS OR SILVER RETRIEVERS

K Number: K800444 · Decision Mar 5, 1980
Classifications
1
FEI Numbers
373
Registration Numbers
373
Same Product Code
14
Applicant Total
28
Review Days
6

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Basic Information

Device Name
GOLDEN RETRIEVERS OR SILVER RETRIEVERS
K Number
K800444
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Instrument Makar, Inc.
Date Received
February 28, 1980
Decision Date
March 5, 1980
Product Code
HXB
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
HXB Probe

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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
K930980 INSTRUMENT MAKAR PERFIX INTERFERENCE BONE SCREW
Search all 28 clearances from Instrument Makar, Inc. →