510(k) K853186
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