510(k) K800898

SILASTIC BONE PLUG H.P.(CEMENT RESTRICT) by Dow Corning Corp. Healthcare Industries Materials — Product Code JDS

K800898 is an FDA 510(k) premarket notification submitted by Dow Corning Corp. Healthcare Industries Materials for the device "SILASTIC BONE PLUG H.P.(CEMENT RESTRICT)". The FDA issued a decision of Substantially Equivalent on May 2, 1980. The device falls under product code JDS (Nail, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Dow Corning Corp. Healthcare Industries Materials has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 2, 1980
Date Received
April 18, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nail, Fixation, Bone
Device Class
Class II
Regulation Number
888.3030
Review Panel
OR
Submission Type