FDA 510(k) Applications Submitted by Jason Blain
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K040276 |
02/05/2004 |
QUANTUM CEMENT RESTRICTOR |
QUANTUM ORTHOPEDICS |
| K050449 |
02/22/2005 |
QUANTUM VERTEBRAL BODY REPLACEMENT |
QUANTUM ORTHOPEDICS, INC. |
| K060491 |
02/24/2006 |
QUANTUM ANTERIOR CERVICAL PLATE SYSTEM |
QUANTUM ORTHOPEDICS, INC. |
| K141372 |
05/27/2014 |
MERCURY SPINAL SYSTEM |
SPINAL ELEMENTS, INC. |
| K251644 |
05/29/2025 |
ProAM ALIF System |
Pro Surgical, Inc. |
| K991882 |
06/02/1999 |
NEXFLEX TOTAL KNEE SYSTEM |
NEXMED, INC. |
| K061576 |
06/07/2006 |
MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT SYSTEM |
QUANTUM ORTHOPEDICS, INC. |
| K992350 |
07/14/1999 |
PYLON INTRAMEDULLAARY NAIL SYSTEM |
ALPHATEC MFG., INC. |
| K242517 |
08/23/2024 |
ProAM ACDF System |
Pro Surgical, Inc. |
| K052641 |
09/26/2005 |
MODIFICATION TO: QUANTUM VERTEBRAL BODY REPLACEMENT |
QUANTUM ORTHOPEDICS, INC. |
| K993513 |
10/18/1999 |
DELTALOC ANTERIOR CERVICAL PLATE SYSTEM |
ALPHATEC MFG., INC. |
| K993873 |
11/15/1999 |
ALPHATEC EXTERNAL FIXATION SYSTEM COMPRESSION/DISTRACTION ROD |
ALPHATEC MFG., INC. |
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