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

PDS (POLYDIOXANON) ABSORBABLE PIN

K Number: K864912 · Decision Jul 9, 1987
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
206
Review Days
206

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Basic Information

Device Name
PDS (POLYDIOXANON) ABSORBABLE PIN
K Number
K864912
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Johnson & Johnson Professionals, Inc.
Date Received
December 15, 1986
Decision Date
July 9, 1987
Product Code
HTY
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
HTY Pin, Fixation, Smooth

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