Atlas FDA

INTEROSSEOUS NEEDLE

FDA 510(k) clearance K761206 · decided 1976-12-13

Clearance details

K-number
K761206
Device name
INTEROSSEOUS NEEDLE
Applicant
Smith & Nephew, Mpl Division
Decision
Substantially Equivalent
Date received
1976-12-07
Decision date
1976-12-13
Days to decision
6 days
Clearance type
Traditional
Product code
DZM
Device class
1
Regulation number
872.4730
Medical specialty
Dental
Advisory committee
Dental
Location
Mchenry, IL, 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
X-TIP INTRAOSSEOUS PERFORATOR (K990511)Schiff & Co.1999-04-27
JENKER NEEDLE STICK PROTECTOR (K920758)Dentsply Intl.1992-04-28
ASEPTIC DENTAL TECH. TOTAL TREATMENT SYSTEM (K914562)Aseptic Dental Technologies, Inc.1992-03-09
SAFETY PLUS DENTAL INJECTION NEEDLE (K913573)Specialites Septodont1991-11-07
DENTAL NEEDLE PROTECTIVE SYSTEM (K910475)Health Technology Systems, Inc.1991-09-13
STABIDENT LOCAL ANESTHESIA SYSTEM (K910446)Fairfax Dental, Inc.1991-06-03
SAFE-T-CAP NEEDLE COVER (K896219)Ausmedics Pty , Ltd.1990-01-22
NIPRO DENTAL NEEDLE (K894373)Pharma-Plast USA, Inc.1989-10-13
DENTAL NEEDLE (CARTRIDGE TYPE) (K870921)Churchill Corp.1987-04-03
TERUMO DENTAL NEEDLES (K864970)Terumo Medical Corp.1987-03-10
EXEL DENTAL NEEDLE (K861150)Exel Intl.1986-04-11
SEPTOJECT STERILE DISPOSABLE INJECTION NEEDLE (K851524)Specialites Septodont1985-09-23

Recalls involving this device

No recalls on record reference this clearance.