Product code KAM— General, Plastic Surgery
ETHMOID SINUS SPACER
- Classification name
- Cannula, Sinus
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 19
- First cleared
- Most recent
Market context for product code KAM
FDA has cleared devices under product code KAM between 1982 and 2011, filed by 6 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 2011
- 2010
- 2009
- 2008
- 2007
- 2006
- 2005
- 2000
- 1997
- 1995
- 1993
- 1991
- 1990
- 1982
Top applicants under product code KAM
Recent clearances under product code KAM
- K110687 — RELIEVA STRATUS PRO MICROFLOW SPACER (FRONTAL)
- K093594 — MODIFICATION TO RELIEVA STRATUS MICROFLOW SPACER
- K083574 — RELIEVA STRATUS MICROFLOW SPACER
- K072891 — SINUS SPACER
- K073041 — RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER
- K071845 — RELIEVA LUMA SINUS ILLUMINATION SYSTEM, MODEL SIS-100A
- K062458 — ETHMOID SINUS SPACER
- K060974 — RELIENT NAVIGATION DEVICE
- K050340 — MICROMEDICS SPHENOID SINUS STENT
- K994262 — FRONTAL SINUS TREPHINATION CANNULA
- K973273 — XOMED T-STENT, FRONTAL SINUS STENT
- K951803 — ROSSITER SINUS STENT
- K951066 — RAINS FRONTAL SINUS STENT
- K942495 — SINOJET MAXILLARY SINUS PUNCTURE & IRRIGATION SYSTEM
- K922902 — SALMAN SINUS BUTTON
- K922145 — SINOJECT MAXILLARY SINUS PUNCTURE & IRRIGATION SYS
- K912418 — SHIKANI MIDDLE MEATAL ANTROSTOMY VENT TUBE
- K896630 — SINOVENT MAXILLARY SINUS DRAINAGE SYSTEM
- K813474 — MAXILL-AIR SINUS VENTILATION TUBE
Data sourced from openFDA. This site is unofficial and independent of the FDA.