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

CEBOPLANE

K Number: K933933 · Decision Apr 15, 1994
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
20
Applicant Total
10
Review Days
247

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Basic Information

Device Name
CEBOPLANE
K Number
K933933
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synvasive Technology, Inc.
Date Received
August 11, 1993
Decision Date
April 15, 1994
Product Code
HTZ
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
HTZ Instrument, Cutting, Orthopedic

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Other Clearances by Synvasive Technology, Inc.

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K070108 ELIBRA DYNAMIC KNEE BALANCER
K972508 SURGICAL BURS AND SURGICAL DRILL BITS
K961522 KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN
K950009 POWERGRIP(TM) COMPRESSION FIXATION DEVICE
K934336 SPINALPLANE
K930573 SYNVASIVE CERAMIC SUTTING BLOCK
K932869 ARTHROPLANE
K931737 HEDLEYL INTRAMEDULLARY PREPARATION BRUSH