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

MEMOGRAPH; OSSTAPLE - NEUROSURGICAL USES FOR CRANIOFACIAL FRACTURES AND CRANIOPLASTY FOR THE MEMOGRAPH STAPLE SYSTEM

K Number: K001353 · Decision Mar 13, 2001
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
6
Applicant Total
13
Review Days
319

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Basic Information

Device Name
MEMOGRAPH; OSSTAPLE - NEUROSURGICAL USES FOR CRANIOFACIAL FRACTURES AND CRANIOPLASTY FOR THE MEMOGRAPH STAPLE SYSTEM
K Number
K001353
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5360
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomedical Ent., Inc.
Date Received
April 28, 2000
Decision Date
March 13, 2001
Product Code
HBW
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
HBW Fastener, Plate, Cranioplasty

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HBW), ordered by most recent decision date.

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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
K001354 MEMOGRAPH; OSSTAPLE - ORTHOPEDIC USES FOR SMALL BONE AND FRAGMENT FIXATION FOR THE MEMOGRAPH STAPLE SYSTEM
K001219 MEMOGRAPH; OSSTAPLE - ORAL AND MAXILLIOFACIAL PROCEDURES 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. →