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

MICRO SURGICAL INSTRUMENT SYSTEM

K Number: K884492 · Decision Nov 16, 1988
Classifications
1
FEI Numbers
67
Registration Numbers
67
Same Product Code
55
Applicant Total
7
Review Days
21

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MICRO SURGICAL INSTRUMENT SYSTEM
K Number
K884492
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Tava Surgical Instruments
Date Received
October 26, 1988
Decision Date
November 16, 1988
Product Code
HSZ
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
HSZ Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment

Similar 510(k) Clearances

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

View all

Other Clearances by Tava Surgical Instruments

K Number Device Name
K935367 TAVA WIRE-DRIVER
K940109 TAVA K-WIRE
K885273 MICRO SURGICAL INSTRUMENT SYSTEM
K872475 SURGICAL BUR
K863788 SAWBLADE
K854543 PULSE LAVAGE