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

STERNAL POWER AWL

K Number: K873766 · Decision Nov 14, 1988
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
28
Applicant Total
14
Review Days
425

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Basic Information

Device Name
STERNAL POWER AWL
K Number
K873766
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Bowen & Company, Inc.
Date Received
September 16, 1987
Decision Date
November 14, 1988
Product Code
KIJ
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
KIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

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Other Clearances by Bowen & Company, Inc.

K Number Device Name
K896898 BOWEN ELECTRODE SKIN PREPATORY CLEANSER
K896538 DISPOSABLE 45 DEGREE SHAVER
K872098 CREMEEN ALVEOLAR BONE CALIPER
K871325 BOWEN REUSEABLE/DISPOSABLE ELECTRODE
K870882 45 DEGREE SHAVER
K870881 LOOSE BODY GRASPERS
K863146 BOWEN SUTURE PASSER
K863148 BOWEN KNOT PASSER
K863149 BOWEN PROBE
K863147 GLENOID DRILL
Search all 14 clearances from Bowen & Company, Inc. →