FDA 510(k) Applications Submitted by ICOTEC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100305 | 02/03/2010 | ETURN SPINAL IMPLANT MODEL ETURN XX-12; ETURN XX-16 WHERE XX=07, 09, 11, 13, OR 15 AND ETURN XX-12 K; ETURN XX-16 K WHER | ICOTEC |
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