FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

KNOWLES PIN

K Number: K905344 · Decision Dec 11, 1990
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
93
Applicant Total
23
Review Days
13

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
KNOWLES PIN
K Number
K905344
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
O'Tec Corp.
Date Received
November 28, 1990
Decision Date
December 11, 1990
Product Code
JDW
Advisory Committee
Orthopedic
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
JDW Pin, Fixation, Threaded

Similar 510(k) Clearances

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

View all

Other Clearances by O'Tec Corp.

K Number Device Name
K943293 SCC22/ SCC26 SHOWER COMMODE CHAIR
K910093 FUTURA FEMORAL HIP STEM
K905333 U.S. TYPE CRUCIATE SLOT BONE SCREW
K905347 HAGIE PIN
K905357 CORTICAL BONE SCREW (EUROPEAN STYLE)
K905358 CANCELLOUS SCREW
K905355 BROAD SELF-COMPRESSING PLATE
K905348 HANSEN-STREET TYPE INTRAMEDULLARY NAIL
K905362 BARBED SQUARE STAPLE
K905338 SIDE PLATE
Search all 23 clearances from O'Tec Corp. →