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

SURGICAL BURS AND SURGICAL DRILL BITS

K Number: K972508 · Decision Aug 26, 1997
Classifications
1
FEI Numbers
387
Registration Numbers
387
Same Product Code
75
Applicant Total
10
Review Days
54

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Basic Information

Device Name
SURGICAL BURS AND SURGICAL DRILL BITS
K Number
K972508
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synvasive Technology, Inc.
Date Received
July 3, 1997
Decision Date
August 26, 1997
Product Code
HWE
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

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