Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Innerspace with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 2, 2012: HUMMINGBIRD SUBDURAL H900DS (DRAINAGE AND ICP), HUMMINGBIRD SUBDURAL- H800S (ICP ONLY).
| Date | Record | Source |
|---|---|---|
| May 2, 2012 | HUMMINGBIRD SUBDURAL H900DS (DRAINAGE AND ICP), HUMMINGBIRD SUBDURAL- H800S (ICP ONLY)K113088 · GWM | 510(k) clearances |
| Sep 29, 2009 | SYNERGYK083378 · GWM | 510(k) clearances |
| Apr 29, 2008 | MPS OXIPORT AND MPS OXIPORT PLUSK072379 · GWM | 510(k) clearances |
| Mar 1, 2005 | MPS (OR MPS-T)K041838 · GWM | 510(k) clearances |
| Sep 9, 2002 | ACT III VENTRICULAR CATHETERK013705 · GWM | 510(k) clearances |
| Mar 8, 2002 | ACT 11 MP VENTRICULAR CATHETERK013005 · HCA | 510(k) clearances |
| Jun 28, 2001 | ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETERK010422 · GWM | 510(k) clearances |
| Jun 15, 2001 | ACTI-ICP MONITORING SYSTEMK003905 · GWM | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
