510(k) K853186

SILASTIC INFLATABLE BONE PLUG H.P. by Dow Corning Corp. Healthcare Industries Materials — Product Code LZN

K853186 is an FDA 510(k) premarket notification submitted by Dow Corning Corp. Healthcare Industries Materials for the device "SILASTIC INFLATABLE BONE PLUG H.P.". The FDA issued a decision of Substantially Equivalent on September 24, 1985. The device falls under product code LZN (Cement Obturator), a Class II device regulated under 21 CFR 878.3300. Dow Corning Corp. Healthcare Industries Materials has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 24, 1985
Date Received
July 30, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cement Obturator
Device Class
Class II
Regulation Number
878.3300
Review Panel
OR
Submission Type