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

LACTOSORB PANELS AND FASTENERS

K Number: K980927 · Decision Jun 5, 1998
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
441
Review Days
86

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Basic Information

Device Name
LACTOSORB PANELS AND FASTENERS
K Number
K980927
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet, Inc.
Date Received
March 11, 1998
Decision Date
June 5, 1998
Product Code
JEY
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JEY Plate, Bone

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