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

MEMOGRAPH; OSSTAPLE - ORAL AND MAXILLIOFACIAL PROCEDURES FOR THE MEMOGRAPH STAPLE SYSTEM

K Number: K001219 · Decision Jun 21, 2000
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
13
Review Days
65

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Basic Information

Device Name
MEMOGRAPH; OSSTAPLE - ORAL AND MAXILLIOFACIAL PROCEDURES FOR THE MEMOGRAPH STAPLE SYSTEM
K Number
K001219
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomedical Ent., Inc.
Date Received
April 17, 2000
Decision Date
June 21, 2000
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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Other Clearances by Biomedical Ent., Inc.

K Number Device Name
K133844 SPEED TRIAD
K133780 SPEED XL
K131640 SMOOTH OR THREADED METALLIC BONE FASTENER
K102107 OSSTAPLE CHILL
K091951 HAMMERLOCK
K023203 OSSTAPLE
K001353 MEMOGRAPH; OSSTAPLE - NEUROSURGICAL USES FOR CRANIOFACIAL FRACTURES AND CRANIOPLASTY FOR THE MEMOGRAPH STAPLE SYSTEM
K001354 MEMOGRAPH; OSSTAPLE - ORTHOPEDIC USES FOR SMALL BONE AND FRAGMENT FIXATION FOR THE MEMOGRAPH STAPLE SYSTEM
K993714 MEMOGRAPH STAPLE, WARM SYSTEM
K971782 BONE AND MARROW COLLECTION SYSTEM KIT
Search all 13 clearances from Biomedical Ent., Inc. →