Atlas FDA

SURGICAL BUR

FDA 510(k) clearance K950449 · decided 1995-03-01

Clearance details

K-number
K950449
Device name
SURGICAL BUR
Applicant
Transidyne General Corp.
Decision
Substantially Equivalent
Date received
1995-02-03
Decision date
1995-03-01
Days to decision
26 days
Clearance type
Traditional
Product code
GFF
Device class
1
Regulation number
878.4820
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Spartanburg, SC, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ANSPACH SHIELDED ATTACHMENT (K974025)The Anspach Effort, Inc.1998-07-06
SURGICAL BUR (K943758)Komet Medical1994-08-22
BURRS (K934583)American Medical Specialties, Inc.1994-01-26
MICRO-AIRE CUTTERS FOR MIDAS-REX INSTRUMENTS (K894438)Micro-Aire Surgical Instruments, Inc.1989-08-21
DANEK IRRIGATING BURR (DIB) SET (K890090)Danek Medical, Inc.1989-01-24
KOMET SURGICAL BUR (K883255)Komet Medical, Div. of Brasseler USA I, L.P.1988-09-15
SURGICAL BURS (K880859)New England Surgical Instrument Corp.1988-03-21
SURGICAL BURS (K880706)Nuell Air Equipment & Hospital Supplies, Inc.1988-02-26
SURGICAL BUR (K872475)Tava Surgical Instruments1987-07-02
MICRO-AIRE REPLACE OTOLOGY BURS/ZIM HALL SUR INSTR (K862852)Micro-Aire Surgical Instruments, Inc.1986-08-11
BURS FOR MICRO SURGICAL DRILL SYSTEM (K853658)Acumed Instruments Corp.1985-09-24
MICRO-AIRE GENERIC BURS & DRILLS (K850497)Micro-Aire Surgical Instruments, Inc.1985-03-01

Recalls involving this device

No recalls on record reference this clearance.