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

MICRO-SURGICAL POWER INSTRUMENT SYS.

K Number: K821487 · Decision Jul 2, 1982
Classifications
1
FEI Numbers
304
Registration Numbers
304
Same Product Code
26
Applicant Total
5
Review Days
45

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Basic Information

Device Name
MICRO-SURGICAL POWER INSTRUMENT SYS.
K Number
K821487
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Spire Medical, Inc.
Date Received
May 18, 1982
Decision Date
July 2, 1982
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GFA), ordered by most recent decision date.

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Other Clearances by Spire Medical, Inc.

K Number Device Name
K821485 DERMABRADERS
K821486 MICRO DRILLS
K802463 MICRO-SURGICAL POWER INSTRUMENT SYSTEM
K802503 MICRO-SUGICAL POWER INSTRUMENT SYSTEM