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

BONE AND MARROW COLLECTION SYSTEM KIT

K Number: K971782 · Decision Jul 29, 1997
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
40
Applicant Total
13
Review Days
76

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Basic Information

Device Name
BONE AND MARROW COLLECTION SYSTEM KIT
K Number
K971782
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Biomedical Ent., Inc.
Date Received
May 14, 1997
Decision Date
July 29, 1997
Product Code
GEY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEY Motor, Surgical Instrument, Ac-Powered

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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
K001219 MEMOGRAPH; OSSTAPLE - ORAL AND MAXILLIOFACIAL PROCEDURES FOR THE MEMOGRAPH STAPLE SYSTEM
K993714 MEMOGRAPH STAPLE, WARM SYSTEM
Search all 13 clearances from Biomedical Ent., Inc. →