Atlas FDA

CRANIO BLADES AND WIRE PASS DRILL

FDA 510(k) clearance K861876 · decided 1986-05-30

Clearance details

K-number
K861876
Device name
CRANIO BLADES AND WIRE PASS DRILL
Applicant
New England Surgical Instrument Corp.
Decision
Substantially Equivalent
Date received
1986-05-15
Decision date
1986-05-30
Days to decision
15 days
Clearance type
Traditional
Product code
GFA
Device class
1
Regulation number
878.4820
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Rockland, MA, 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
GRAFT HARVESTING SAWBLADES (K971978)Wrightmedicaltechnologyinc1997-06-18
STRYKER SAGITTAL SAW ATTACHMENT (K954483)Stryker Instruments1996-01-30
WRIGHT MEDICAL TECHNOLOGY SAWBLADES (K955229)Wrightmedicaltechnologyinc1996-01-18
DISPOSABLE & REUSABLE SURGICAL CUTTING TOOLS (K953012)Boston Surgical Products, Inc.1995-07-12
SURGICAL SAW BLADES (K950403)Transidyne General Corp.1995-02-21
RE-SHARPENABLE SAW BLADES (K940501)Adven Medical1994-06-28
BUR, SURGICAL, GENERAL & PLASTIC SURGERY (K933595)Omega Surgical Instruments, Inc.1994-03-16
SARNS STERNAL SAW II, STERNAL SAW II BLADE, SARNS SAW BLADES-NON-STERILE BULK PACK (K935391)3M Health Care, Sarns1994-02-24
SURGICAL SAW BLADES (K934603)American Medical Specialties, Inc.1994-02-22
SNAP OSCILLATING SAW (K931769)Surgiquip, Inc.1994-01-27
OSCILLATING BONE SAW BLADE, 6200 SERIES (K934390)Boehringer Laboratories1994-01-26
INTERMEDICS ORTHOPEDICS SAW BLADE (K931210)Intermedics Orthopedics1993-11-18

Recalls involving this device

No recalls on record reference this clearance.