The following data is part of a premarket notification filed by Buckman Co., Inc. with the FDA for Ace Mos Saw And The Ace Mos Spine Saw.
| Device ID | K862504 |
| 510k Number | K862504 |
| Device Name: | ACE MOS SAW AND THE ACE MOS SPINE SAW |
| Classification | Instrument, Surgical, Sonic And Accessory/attachment |
| Applicant | BUCKMAN CO., INC. 921 CALLE VERDE Martinez, CA 94553 |
| Contact | David W Schlerf |
| Correspondent | David W Schlerf BUCKMAN CO., INC. 921 CALLE VERDE Martinez, CA 94553 |
| Product Code | JDX |
| CFR Regulation Number | 888.4580 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-07-01 |
| Decision Date | 1986-08-07 |