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

SURGICAL SAW BLADES

K Number: K950403 · Decision Feb 21, 1995
Classifications
1
FEI Numbers
304
Registration Numbers
304
Same Product Code
26
Applicant Total
21
Review Days
21

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Basic Information

Device Name
SURGICAL SAW BLADES
K Number
K950403
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
Transidyne General Corp.
Date Received
January 31, 1995
Decision Date
February 21, 1995
Product Code
GFA
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
GFA Blade, Saw, General & Plastic Surgery, Surgical

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Other Clearances by Transidyne General Corp.

K Number Device Name
K961217 BODILY FLUID DISPOSAL KIT
K955658 LACERATION TRAY
K950773 PROPHYLAXIS PACK
K950743 ORAL PROCEDURE PACK
K950449 SURGICAL BUR
K924811 I.V. START KIT
K924243 TRACHEOSTOMY CARE KIT
K922339 SUTURE REMOVAL KIT
K922041 PRIMARY SURGICAL DRESSING TRAY
K897133 MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT
Search all 21 clearances from Transidyne General Corp. →