The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Miig Sr.
| Device ID | K060011 |
| 510k Number | K060011 |
| Device Name: | MIIG SR |
| Classification | Filler, Bone Void, Calcium Compound |
| Applicant | WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
| Contact | Brian J Young |
| Correspondent | Brian J Young WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
| Product Code | MQV |
| CFR Regulation Number | 888.3045 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-01-03 |
| Decision Date | 2006-02-27 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00840420140821 | K060011 | 000 |
| 00840420135599 | K060011 | 000 |
| 00840420135605 | K060011 | 000 |
| 00840420135612 | K060011 | 000 |
| 00840420135629 | K060011 | 000 |
| 00840420137272 | K060011 | 000 |
| 00840420137289 | K060011 | 000 |
| 00840420137296 | K060011 | 000 |
| 00840420140791 | K060011 | 000 |
| 00840420135582 | K060011 | 000 |