Integra® Miltex® POLYGLYCOLIC ACID POLYMER, Sterile Absorbable Sutures, Suture Length: 27" (69cm), 5-0 (1.0 Metric), Cutting Edge 3/8 Circle, Reverse Cut, C-6, 19mm
Who Else Makes It
Concentrated in Shanghai (1), Shandong (1), Beijing (1).
Record
Regulatory record for Miltex® | Listed by | Integra LifeSciences Production Corporation, United States |
| FDA product code | GAM |
| Device type | Suture, Absorbable, Synthetic, Polyglycolic Acid |
| Device class | Class 2 |
| Regulation | 21 CFR 878.4493 |
| Establishment | Contract manufacturer, Specification developer, Manufacturer |
| 510(k) | K033762 |
| Record published | 2015-09-22 |
| Record revised | 2026-05-28 (version 8) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: Do not use if package is damaged |
| Packaging | Box of 12 |
| Sizes | Length 27 in; length 69 cm |
| Distribution end date | 2016-12-22 |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.