Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K972367
Device Classification Name
Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment
More FDA Info for this Device
510(K) Number
K972367
Device Name
Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment
Applicant
STRYKER INSTRUMENTS
4100 EAST MILHAM AVE.
KALAMAZOO, MI 49001 US
Other 510(k) Applications for this Company
Contact
MELISSA HARRIGER
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
KIJ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/25/1997
Decision Date
09/04/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact