Stablecut® 506113
GUDID 00880304537880
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.
Surgical saw blade, reciprocating, single-use| Primary Device ID | 00880304537880 |
| NIH Device Record Key | aabfdbd8-cccd-490a-a736-a1522a37e6d2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Stablecut® |
| Version Model Number | 506113 |
| Catalog Number | 506113 |
| Company DUNS | 137354267 |
| Company Name | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
Device Dimensions
| Width | 10 Millimeter |
| Length | 70 Millimeter |
| Device Size Text, specify | 0 |
| Width | 10 Millimeter |
| Length | 70 Millimeter |
| Device Size Text, specify | 0 |
| Width | 10 Millimeter |
| Length | 70 Millimeter |
| Device Size Text, specify | 0 |
| Width | 10 Millimeter |
| Length | 70 Millimeter |
| Device Size Text, specify | 0 |
| Width | 10 Millimeter |
| Length | 70 Millimeter |
| Device Size Text, specify | 0 |
| Width | 10 Millimeter |
| Length | 70 Millimeter |
| Device Size Text, specify | 0 |
| Width | 10 Millimeter |
| Length | 70 Millimeter |
| Device Size Text, specify | 0 |
| Width | 10 Millimeter |
| Length | 70 Millimeter |
| Device Size Text, specify | 0 |
| Width | 10 Millimeter |
| Length | 70 Millimeter |
| Device Size Text, specify | 0 |
| Width | 10 Millimeter |
| Length | 70 Millimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304537880 [Primary] |
FDA Product Code
| GFA | BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-11 |
| Device Publish Date | 2022-10-03 |
On-Brand Devices [Stablecut®]
Trademark Results [Stablecut]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 STABLECUT 85211274 3990180 Live/Registered |
Synvasive Technology, Inc. 2011-01-05 |
 STABLECUT 76393707 2672143 Dead/Cancelled |
SYNVASIVE TECHNOLOGY, INC. 2002-04-09 |
 STABLECUT 74299253 1758178 Dead/Cancelled |
Sierra Surgical, Inc. 1992-07-28 |
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