The following data is part of a premarket notification filed by Medicrea Technologies with the FDA for C-jaws Cervical Compressive Mini Frame.
| Device ID | K072040 |
| 510k Number | K072040 |
| Device Name: | C-JAWS CERVICAL COMPRESSIVE MINI FRAME |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| Applicant | MEDICREA TECHNOLOGIES 1001 OAKWOOD BLVD. Round Rock, TX 78681 |
| Contact | J.d. Webb |
| Correspondent | J.d. Webb MEDICREA TECHNOLOGIES 1001 OAKWOOD BLVD. Round Rock, TX 78681 |
| Product Code | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-07-25 |
| Decision Date | 2007-08-03 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 03613720192190 | K072040 | 000 |
| 03613720192084 | K072040 | 000 |
| 03613720192077 | K072040 | 000 |
| 03613720192060 | K072040 | 000 |
| 03613720192053 | K072040 | 000 |
| 03613720192046 | K072040 | 000 |
| 03613720192039 | K072040 | 000 |
| 03613720192022 | K072040 | 000 |
| 03613720192015 | K072040 | 000 |
| 03613720192091 | K072040 | 000 |
| 03613720192107 | K072040 | 000 |
| 03613720192183 | K072040 | 000 |
| 03613720192176 | K072040 | 000 |
| 03613720192169 | K072040 | 000 |
| 03613720192152 | K072040 | 000 |
| 03613720192145 | K072040 | 000 |
| 03613720192138 | K072040 | 000 |
| 03613720192121 | K072040 | 000 |
| 03613720192114 | K072040 | 000 |
| 03613720192008 | K072040 | 000 |