The following data is part of a premarket notification filed by Linvatec Corp. with the FDA for Revo Rotator Cuff Repair System.
| Device ID | K941691 |
| 510k Number | K941691 |
| Device Name: | REVO ROTATOR CUFF REPAIR SYSTEM |
| Classification | Arthroscope |
| Applicant | LINVATEC CORP. 11311 CONCEPT BLVD. Largo, FL 33773 |
| Contact | Carole A Weideman |
| Correspondent | Carole A Weideman LINVATEC CORP. 11311 CONCEPT BLVD. Largo, FL 33773 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-04-06 |
| Decision Date | 1994-09-06 |